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RESIDENCY PROGRAM NEWS

 

Our four-year ACGME AP/CP Residency Program is fully accredited with no citations.

Effective January 26, 2015, our AP/CP Training Program received continued accreditation with no citations by the Residency Review Committee for Pathology of the ACGME.  Our accreditation was extended until 2017. 

Performance in 2014 American Board of Pathology Examinations (AP / CP)
We are delighted to report that almost all of our graduates who have completed our program since 2002 have passed the American Board of Pathology AP and CP exams! We congratulate our graduates on their outstanding performance!

Outstanding Performance in 2014 ASCP Residents In-Service Examination (RISE)
We are delighted to report that our first, second and third year residents performed at the 95th percentile or better overall as compared with their peers nationally. We congratulate our residents for their outstanding performance. At the end of the day, it is their hard work and determination that has paid off.

Four New Residents Joined Our Program July 1, 2014
We welcome our four new residents and look forward to working with each of them in the years ahead:

Dr. Nigar Anjuman received her MB, BS in 2010 from Rawalpindi Medical College in Pakistan.  Dr. Anjuman did research in the Department of Pathology of the University of Maryland prior to joining our program.

Dr. Joshua Kagan received his BA in Chemistry with a minor in Economic Policy from New York University.  He earned his MD in 2013 from St. George's University in Grenada. Prior to joining our program, Dr. Kagan spent one year in a residency program in Internal Medicine.

 

Dr. Amir Momeni received his MD in 2010 from Isfahan University of Medical Sciences in Iran.  Dr. Momeni is the author of several peer reviewed publications.  He was a correspondent for PBS-Frontline prior to joining our program.

 

Dr. Jose Victor Scarpa Carniello received his MD in 2011 from the Faculdade de Ciencias Medicas da Santa Casa de Sao Paulo in Brazil.  Dr. Scarpa Carniello was a research scholar at Brown University and a research fellow at Memorial Sloan-Kettering Cancer Center prior to joining our program. 

 

 

Recent Resident Publications

Berulava, Giorgi

Gynecol Oncol Case Rep. 2013 Jun 10;6:1-3. doi: 10.1016/j.gynor.2013.06.001. eCollection 2013.

Port-site recurrence in a patient undergoing robotic hysterectomy and lymph node dissection for endometrioid adenocarcinoma of the uterus.

Alagkiozidis I1, Zhining NT1, Berulava G2, Abulafia O1, Salame G1.

2Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York, NY, USA.

Abstract

•We present a case of port-site recurrence of endometrioid adenocarcinoma after robotic hysterectomy and staging.•Port-site recurrence is commonly an indicator of multifocal disease with poor prognosis.•Surgical techniques that decrease the risk of this complication should be implemented.

PMID: 24371704 [PubMed] PMCID: PMC3862220 

 Fig. 1Fig. 2Fig. 3

 

Garcia, Rafael

J Clin Lab Anal. 2012 Sep;26(5):372-5. doi: 10.1002/jcla.21533.

Stability of electrolyte determinations on the Siemens Advia 1800 analyzer.

Garcia R1, Li G, Wang Z, Cabanero M, Pincus MR.

1Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York, NY, USA.

Abstract

BACKGROUND:

It is sometimes necessary for the laboratory to re-test samples for critical serum electrolyte levels. It is important to assure reproducibility of results when testing is performed on stored, refrigerated samples. We have tested the reproducibility of results for the critical electrolytes, Na, K, Cl and Ca, from ten randomly selected patients'sera over our maximum storage period of nine (9) days on the Siemens Advia 1800 analyzer. The ranges for each electrolyte were 131-150 meq/L (Na), 3.4-5.2 meq/L (K), 101-123 meq/L (Cl) and 7.3-9.9 mg/dL (Ca).

METHODS:

We used ion-selective electrodes for Na, K and Cl and the ortho-cresolphthalein dye method for Ca.

RESULTS:

We find that the reproducibility of determinations for all of these electrolytes was excellent, i.e. the coefficients of variation for each electrolyte determination for each patient were low.

CONCLUSION:

The methods of measurement for these electrolytes on the Advia 1800 are reliable and reproducible.

© 2012 Wiley Periodicals, Inc.

PMID: 23001983

 

Gilani, Ahmed

Proc Natl Acad Sci U S A. 2014 May 20;111(20):7450-5. doi: 10.1073/pnas.1316488111. Epub 2014 May 2.

Interneuron precursor transplants in adult hippocampus reverse psychosis-relevant features in a mouse model of hippocampal disinhibition.

Gilani AI1, Chohan MO2, Inan M3, Schobel SA2, Chaudhury NH4, Paskewitz S4, Chuhma N2, Glickstein S5, Merker RJ4, Xu Q6, Small SA7, Anderson SA8, Ross ME9, Moore H10.

1New York State Psychiatric Institute, New York, NY 10032;Department of Biological Sciences, Columbia University, New York, NY 10027; Departments of. (currently Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York, NY, USA.

Abstract

GABAergic interneuron hypofunction is hypothesized to underlie hippocampal dysfunction in schizophrenia. Here, we use the cyclin D2 knockout (Ccnd2(-/-)) mouse model to test potential links between hippocampal interneuron deficits and psychosis-relevant neurobehavioral phenotypes. Ccnd2(-/-) mice show cortical PV(+) interneuron reductions, prominently in hippocampus, associated with deficits in synaptic inhibition, increased in vivo spike activity of projection neurons, and increased in vivo basal metabolic activity (assessed with fMRI) in hippocampus. Ccnd2(-/-) mice show several neurophysiological and behavioral phenotypes that would be predicted to be produced by hippocampal disinhibition, including increased ventral tegmental area dopamine neuron population activity, behavioral hyperresponsiveness to amphetamine, and impairments in hippocampus-dependent cognition. Remarkably, transplantation of cells from the embryonic medial ganglionic eminence (the major origin of cerebral cortical interneurons) into the adult Ccnd2(-/-) caudoventral hippocampus reverses these psychosis-relevant phenotypes. Surviving neurons from these transplants are 97% GABAergic and widely distributed within the hippocampus. Up to 6 mo after the transplants, in vivo hippocampal metabolic activity is lowered, context-dependent learning and memory is improved, and dopamine neuron activity and the behavioral response to amphetamine are normalized. These findings establish functional links between hippocampal GABA interneuron deficits and psychosis-relevant dopaminergic and cognitive phenotypes, and support a rationale for targeting limbic cortical interneuron function in the prevention and treatment of schizophrenia.

PMID: 24794528 [PubMed - indexed for MEDLINE] PMCID: PMC4034251

 

Huang, Tao

Nucleic Acids Res. 2014 Apr;42(8):5347-60. doi: 10.1093/nar/gku140. Epub 2014 Feb 24.

Quaternary arrangement of an active, native group II intron ribonucleoprotein complex revealed by small-angle X-ray scattering.

Gupta K1, Contreras LM, Smith D, Qu G, Huang T, Spruce LA, Seeholzer SH, Belfort M, Van Duyne GD.

1Department of Biochemistry & Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6059, USA, Department of Chemical Engineering, University of Texas at Austin, Austin, TX 78712, USA, Wadsworth Center, NYS Department of Health, Albany, NY 12201, USA, Department of Biological Sciences and RNA Institute, University at Albany, State University of New York, Albany, NY 12222, USA, SUNY Downstate Medical Center, University Hospital, Brooklyn, NY 11203, USA and Children's Hospital of Philadelphia Research Institute, Philadelphia, PA 19104, USA.

Abstract

The stable ribonucleoprotein (RNP) complex formed between the Lactococcus lactis group II intron and its self-encoded LtrA protein is essential for the intron's genetic mobility. In this study, we report the biochemical, compositional, hydrodynamic and structural properties of active group II intron RNP particles (+A) isolated from its native host using a novel purification scheme. We employed small-angle X-ray scattering to determine the structural properties of these particles as they exist in solution. Using sucrose as a contrasting agent, we derived a two-phase quaternary model of the protein-RNA complex. This approach revealed that the spatial properties of the complex are largely defined by the RNA component, with the protein dimer located near the center of mass. A transfer RNA fusion engineered into domain II of the intron provided a distinct landmark consistent with this interpretation. Comparison of the derived +A RNP shape with that of the previously reported precursor intron (ΔA) particle extends previous findings that the loosely packed precursor RNP undergoes a dramatic conformational change as it compacts into its active form. Our results provide insights into the quaternary arrangement of these RNP complexes in solution, an important step to understanding the transition of the group II intron from the precursor to a species fully active for DNA invasion.

PMID: 24567547 [PubMed - indexed for MEDLINE] PMCID: PMC4005650

 Figure 1.

Figure 1.Domain structure, activity and purification of native group II introns. (A) Domain structure of a group II intron. Rendered as squares are the exons (E1 and E2) flanking the group II intron sequence. Denoted with Roman numerals are the six structural domains of the intron. Domain IV contains an ORF that encodes an IEP, also referred to as LtrA. Domain VI contains the catalytic adenosine nucleophile (circled) required for splicing. (B) Splicing reaction carried out by group II introns. Group II introns are excised from flanking exons through a two-step process that is catalyzed by the intron RNA. (C) Purification strategy. Lysates from nisin-induced cells are passed over a chitin resin column to capture LtrA–intein–CBD protein fusion and associated RNA, via a C-terminal chitin-binding domain in the LtrA fusion. I = intein. To facilitate separation (see below), MBP-MS2 (turquoise balls) is added to bind the MS2 tag in the precursor at the 3′ exon (black lollipops). Cleavage of LtrA from the intein with DTT) releases the RNP from the chitin column in both active and precursor forms. Assuming a 1:1 stoichiometry between MBP-MS2 protein (∼50 kD) and its RNA-binding site (21), addition of the MS2 binding protein further increases the size differential between the 12xMS2-containing precursor (∼1.4 MDa) and the spliced lariats form (∼430 kD) of the RNP. This large size differential allows for successful final isolation of the active RNP from the precursor species by sedimentation, using a sucrose cushion gradient.Quaternary arrangement of an active, native group II intron ribonucleoprotein complex revealed by small-angle X-ray scatteringNucleic Acids Res. 2014 April;42(8):5347-5360.

Figure 2.

 

Huang, Tao

RNA. 2013 Nov;19(11):1497-509. doi: 10.1261/rna.039073.113. Epub 2013 Sep 17.

Group II intron-ribosome association protects intron RNA from degradation.

Contreras LM, Huang T, Piazza CL, Smith D, Qu G, Gelderman G, Potratz JP, Russell R, Belfort M.

Abstract

The influence of the cellular environment on the structures and properties of catalytic RNAs is not well understood, despite great interest in ribozyme function. Here we report on ribosome association of group II introns, which are ribozymes that are important because of their putative ancestry to spliceosomal introns and retrotransposons, their retromobility via an RNA intermediate, and their application as gene delivery agents. We show that group II intron RNA, in complex with the intron-encoded protein from the native Lactoccocus lactis host, associates strongly with ribosomes in vivo. Ribosomes have little effect on intron ribozyme activities; rather, the association with host ribosomes protects the intron RNA against degradation by RNase E, an enzyme previously shown to be a silencer of retromobility in Escherichia coli. The ribosome interacts strongly with the intron, exerting protective effects in vivo and in vitro, as demonstrated by genetic and biochemical experiments. These results are consistent with the ribosome influencing the integrity of catalytic RNAs in bacteria in the face of degradative nucleases that regulate intron mobility.

PMID: 24046482 [PubMed - indexed for MEDLINE] PMCID: PMC3851717

 

Li, Geling

Leuk Res. 2014 Sep;38(9):1079-84. doi: 10.1016/j.leukres.2014.07.001. Epub 2014 Jul 14.

A retrospective analysis of ten symptomatic multiple myeloma patients with HIV infection: a potential therapeutic effect of HAART in multiple myeloma.

Li G1, Lewis RD2, Mishra N2, Axiotis CA3.

1Department of Pathology, SUNY Downstate Medical Center, Kings County Hospital Center, Brooklyn, NY, United States

2Department of Haematology/Oncology, SUNY Downstate Medical Center, Kings County Hospital Center, Brooklyn, NY, United States.

3Department of Pathology, SUNY Downstate Medical Center, Kings County Hospital Center, Brooklyn, NY, United States. Electronic address: axiotismd@aol.com.

Abstract

The impact of highly active anti-retroviral therapy (HAART) in multiple myeloma (MM) is unknown. Ten HIV+ and 28 HIV-negative patients were retrospectively identified out of 262 cases of MM diagnosed at Kings County Hospital Center since the introduction of HAART in 1996. The HIV+ MM patients on HAART had superior overall survival (OS) (Fisher exact, p=0.008; log-rank, p=0.012) and progression free survival (PFS) (Fisher exact, p=0.007; log-rank, p=0.009) than the HIV-negative MM patients. HAART alone blocked the production of serum M-protein. We propose that HARRT should be explored for the treatment of both HIV+ and HIV-negative MM patients.

Copyright © 2014 Elsevier Ltd. All rights reserved.

PMID: 25064217

Li, Geling

Ann Clin Lab Sci. 2013 Summer;43(3):278-84.

Comparison of glucose determinations on blood samples collected in three types of tubes.

Li G1, Cabanero M, Wang Z, Wang H, Huang T, Alexis H, Eid I, Muth G, Pincus MR.

1Department of Pathology, SUNY Downstate Medical Center, Brooklyn, NY, 11209, USA.

Abstract

Because of the metabolism of serum glucose in collection tubes containing blood samples, serum glucose levels may be found to decrease over time. Several types of collection tubes have been designed to, at least partially, block glucose metabolism by red blood cells in blood collection tubes that may not be analyzed immediately after blood collection. These include red-top collection tubes with serum separator, grey-top tubes with a fluoride glycolysis inhibitor, and heparin-containing green-top tubes which prevent clot formation. As part of a quality assurance project, we investigated whether glucose levels differed in the three tube types from each of 18 volunteers on a prolonged standing of 4 hours. We then determined the glucose concentrations of all three tubes from each of the 18 volunteers. We used refrigerated samples over a five-day period to determine if the initial values were reproducible. Surprisingly, after standing for four hours at room temperature, we found that the glucose levels in the three tubes from each volunteer were statistically indistinguishable from one another using the two-tailed paired t-test. Also, a linear regression analysis showed that the values of glucose for the three pairs of two tube types were closely correlated with one another, with correlation coefficients of >0.97, slopes close to 1, and Y-intercepts close to 0. These results suggest that blood collection in any of these tubes will render similar values for serum glucose even after standing for four hours. The tubes were then refrigerated at 4°C and re-analyzed after another six hours and then once per day for the next four days. Beginning at the first day at the six-hour determination, the glucose levels in the red- and grey-top tubes were statistically indistinguishable from one another but not in the red- and green-top tubes and in the grey- and green-top tubes. This was due to a steady decrease in the glucose levels in the green-top tubes. The glucose levels in the red- and grey-top tubes from each volunteer remained constant over the five-day period so that the coefficients of variation (CV) were low. In contrast, due to the decrease of glucose levels in the green-top tubes, the CVs for repeated glucose determinations in these tubes were high. Interestingly, a regression analysis of the glucose values for all three sets of paired tubes showed high (> 0.97) correlation coefficients and slopes close to 1. However, a regression analysis of the glucose values in the red- and green-top and grey- and green-top tubes at day five showed Y-intercepts of about -32 suggesting that there is a constant decrease of glucose in the green-top tubes that amounts to approximately 6 mg/dL per day over five days. These results suggest that red-top tubes with serum separator or grey-top tubes with a fluoride glycolysis inhibitor may be used for reproducible glucose determinations.

PMID: 23884222

 

Liang, Jiancong

Clin Neuropathol. 2014 May-Jun;33(3):197-202. doi: 10.5414/NP300702.

Ectopic pituitary adenoma associated with an empty sella presenting with hearing loss: case report with literature review.

Liang J, Libien J, Kunam V, Shao C, Rao C.

Abstract

Ectopic pituitary adenomas are uncommon entities that may pose substantial diagnostic challenges. In the majority of these cases, patients present with endocrine and/or nasal obstruction symptoms. We report the case of an ectopic pituitary adenoma in a 76-year-old man with an empty sella who initially presented with right-sided hearing loss progressing to bilateral hearing loss over the next 4 years. Neuroimaging studies revealed a large, expansile central skull base mass replacing the clivus and sphenoid sinus, and invading the internal auditory canals and inner ear bilaterally. The tumor also involved the floor of the middle cranial fossae and bilateral medial temporal and occipital bones. Histopathologic examination, including immunohistochemical studies, revealed a sparsely granulated lactotroph adenoma. Hearing loss in a patient with ectopic pituitary adenoma constitutes an extremely unusual presentation. This case was further complicated by the presence of an empty sella and the absence of symptoms related to hyperprolactinemia.

PMID: 24447694

Liang, Jiancong

Orbit. 2013 Aug;32(4):266-9. doi: 10.3109/01676830.2013.788672. Epub 2013 May 10.

Pachydermoperiostosis: a rare cause of marked blepharoptosis and floppy eyelid syndrome.

Berdia J1, Tsai FF, Liang J, Shinder R.

1Department of Ophthalmology, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.

Abstract

A 34-year-old African-American man was referred for eyelid swelling and ocular discomfort. He was found to have floppy hypertrophic eyelids and marked bilateral mechanical ptosis that was present since childhood. Systemic examination was significant for furrows on his forehead and scalp, coarse facial features, and enlarged hands and feet with clubbing of the fingers and toes. Radiographic imaging of the long bones demonstrated periostosis, and MRI of the head revealed a pituitary macroadenoma. Pituitary and thyroid hormone levels were normal. The patient was diagnosed with pachydermoperiostosis and a non-secreting pituitary macroadenoma. Bilateral upper lid tightening via wedge resection was followed by bilateral external levator advancement ptosis repair in a staged manner. The patient achieved symptom relief and improved lid position postoperatively.

PMID: 23662673

 

Qin, Jia

J Clin Lab Anal. 2013 Nov;27(6):435-7. doi: 10.1002/jcla.21624.

Stability of BUN and creatinine determinations on the Siemens Advia 1800 analyzer.

Qin J1, Wang H, Rets A, Harari S, Alexis H, Eid I, Pincus MR.

1Department of Pathology and Laboratory Medicine, NY Harbor VA Medical Center 800 Poly Place, Brooklyn, New York; Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York.

Abstract

BACKGROUND:

Serum creatinine values of patients tend to change as a result of the use of different blanks used for creatinine determinations on the Advia 1650. After upgrading the analyzer to the Advia 1800, creatinine values tended to be more reproducible. As part of a quality assurance investigation to test the reproducibilities of creatinine values, we determined serial creatinine values in the sera of 13 patients whose initial values were either in the reference range or elevated (range 0.58-7.8 mg/dl). These values were determined concurrently with serum blood urea nitrogen (BUN) determinations (range 6.0-84.4 mg/dl) as these two analytes are used together in evaluation of renal function.

METHODS:

We determined BUN and creatinine values, using the glutamate dehydrogenase lined enzyme assay system and the Jaffe method, respectively.

RESULTS:

We find that all values for creatinine on samples stored at 4 °C were reproducible as were the corresponding BUN values, which is revealed by low values for the coefficients of variation (CVs), that is, mean CV of 4.55% for creatinine and 2.52% for BUN. One sample with relatively high CV (10.6%) for creatinine was found to have an initial value of 1.1 mg/dl, in the reference range; but, on repeat determinations, the obtained levels were as high as 1.5 mg/dl, above the reference range. BUN values for this sample remained in the reference range, suggesting that no renal disease was present.

CONCLUSION:

We conclude that creatinine and BUN determinations are stable, but occasional spurious creatinine values can occur on the Advia 1800 analyzer.

© 2013 Wiley Periodicals, Inc.

PMID: 24218124

 

Rets, Anton

J Clin Lab Anal. 2013 Nov;27(6):435-7. doi: 10.1002/jcla.21624.

Stability of BUN and creatinine determinations on the Siemens Advia 1800 analyzer.

Qin J1, Wang H, Rets A, Harari S, Alexis H, Eid I, Pincus MR.

1Department of Pathology and Laboratory Medicine, NY Harbor VA Medical Center 800 Poly Place, Brooklyn, New York; Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York.

Abstract

BACKGROUND:

Serum creatinine values of patients tend to change as a result of the use of different blanks used for creatinine determinations on the Advia 1650. After upgrading the analyzer to the Advia 1800, creatinine values tended to be more reproducible. As part of a quality assurance investigation to test the reproducibilities of creatinine values, we determined serial creatinine values in the sera of 13 patients whose initial values were either in the reference range or elevated (range 0.58-7.8 mg/dl). These values were determined concurrently with serum blood urea nitrogen (BUN) determinations (range 6.0-84.4 mg/dl) as these two analytes are used together in evaluation of renal function.

METHODS:

We determined BUN and creatinine values, using the glutamate dehydrogenase lined enzyme assay system and the Jaffe method, respectively.

RESULTS:

We find that all values for creatinine on samples stored at 4 °C were reproducible as were the corresponding BUN values, which is revealed by low values for the coefficients of variation (CVs), that is, mean CV of 4.55% for creatinine and 2.52% for BUN. One sample with relatively high CV (10.6%) for creatinine was found to have an initial value of 1.1 mg/dl, in the reference range; but, on repeat determinations, the obtained levels were as high as 1.5 mg/dl, above the reference range. BUN values for this sample remained in the reference range, suggesting that no renal disease was present.

CONCLUSION:

We conclude that creatinine and BUN determinations are stable, but occasional spurious creatinine values can occur on the Advia 1800 analyzer.

© 2013 Wiley Periodicals, Inc.

PMID: 24218124

 

Wang, Huiying

Case Rep Hematol. 2014;2014:869395. doi: 10.1155/2014/869395. Epub 2014 Jul 17.

Treatment of coexisting chronic neutrophilic leukemia and light chain multiple myeloma with hydroxyurea, bortezomib, and dexamethasone.

Taiwo E1, Wang H1, Lewis R1.

1Kings County Hospital Center, 451 Clarkson Avenue, Brooklyn, NY 11203, USA ; State University of New York, Downstate, Brooklyn, NY, USA.

Abstract

A 63-year-old female was incidentally found to have leukocytosis and referred to the hematology service for evaluation. Complete blood count (CBC) revealed neutrophilia with band predominance and mild thrombocytopenia. Peripheral blood flow cytometry was unremarkable without any evidence of lymphoproliferative disorder or myeloblasts. Bone marrow aspiration and biopsy revealed a markedly hypercellular marrow with myeloid lineage predominance and approximately 10% plasma cells. The monoclonal gammopathy was determined as lambda light chain with a kappa/lambda ratio of 0.06. Cytogenetics revealed normal karyotype, JAK2 kinase was negative, and rearrangement of BCR-ABL1, PDGFRA, PDGFRB, and FGFR1 was negative. The patient was diagnosed with chronic neutrophilic leukemia (CNL) associated with light chain multiple myeloma, complicated by a subdural hemorrhage. She was treated with hydroxyurea and bortezomib/dexamethasone and had complete response with normalization of CBC and kappa/lambda ratio. To the best of our knowledge, we report the first case of chronic neutrophilic leukemia and multiple myeloma treated with bortezomib/dexamethasone.

PMID: 25143840 [PubMed] PMCID: PMC4124778

 Figure 1

Figure 1

Blood smear showing segmented neutrophils with arrow pointing at Döhle bodies.Treatment of Coexisting Chronic Neutrophilic Leukemia and Light Chain Multiple Myeloma with Hydroxyurea, Bortezomib, and DexamethasoneCase Rep Hematol. 2014;2014:869395.

Figure 2

Figure 2

Bone marrow aspiration reveals predominance of myeloid lineage.Treatment of Coexisting Chronic Neutrophilic Leukemia and Light Chain Multiple Myeloma with Hydroxyurea, Bortezomib, and DexamethasoneCase Rep Hematol. 2014;2014:869395.

Figure 3

Figure 3

Bone marrow biopsy reveals a markedly hypercellular marrow.Treatment of Coexisting Chronic Neutrophilic Leukemia and Light Chain Multiple Myeloma with Hydroxyurea, Bortezomib, and DexamethasoneCase Rep Hematol. 2014;2014:869395.

 

2013 and 2014 Conference Presentations

Of 24 residents in our program, over half have presented at national and international conferences during the past two years!

Cochran, Eric

College of American Pathologists, 2014 

Garcia, Rafael

National Association of Medical Examiners, 2013

Huang, Tao

College of American Pathologists, 2014

Li, Geling

College of American Pathologists, 2013

Liang, Jiancong

American Association of Neuropathologists, 2013 & 2014

Lu, Chuanyong

American Society for Clinical Pathology, 2014

College of American Pathologists, 2013

Maglantay, Remegio

College of American Pathologists, 2014

Montecalvo, Joseph

College of American Pathologists, 2013 & 2014

Oza, Twisha

College of American Pathologists, 2014

Qin, Jia

American Society for Clinical Pathology, 2014

United States & Canadian Academy of Pathology, 2014

Rets, Anton

College of American Pathologists, 2013 & 2014

Wang, Huiying

College of American Pathologists, 2014

Zhang, Yan

College of American Pathologists, 2013