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Performance of ACR TI-RADS and the Bethesda System in Predicting Risk of Malignancy in Thyroid Nodules at a Large Children's Hospital and a Comprehensive Review of the Pediatric Literature

Cancers, 2023-08, Vol.15 (15), p.3975

2023

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Neurogenesis and neuronal differentiation in the postnatal frontal cortex in Down syndrome

Acta neuropathologica communications, 2022-06, Vol.10 (1), p.86-86, Article 86

2022

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Underreporting of perforating osteoma cutis: A call for recognition and diagnostic consistency

Journal of cutaneous pathology, 2023-12, Vol.50 (12), p.1033-1035

2023

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Postnatal Cytoarchitecture and Neurochemical Hippocampal Dysfunction in Down Syndrome

Journal of clinical medicine, 2021-07, Vol.10 (15), p.3414

2021

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Diagnostic work-up of hematological malignancies with underlying germline predisposition disorders (GPD)

Seminars in diagnostic pathology, 2023-11, Vol.40 (6), p.443-456

2023

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Over Expression of Insulin-Like Growth Factor Binding Protein 3 in Clear Cell Renal Cell Carcinoma

The Journal of urology, 2008-02, Vol.179 (2), p.445-449

2008

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High Prevalence of Gene Fusions and Copy Number Alterations in Pediatric Radiation Therapy-Induced Papillary and Follicular Thyroid Carcinomas

Thyroid (New York, N.Y.), 2022-04, Vol.32 (4), p.411-420

2022

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Cytochemical Characterization of Cerebrospinal Fluid Macrophage Inclusions in Pediatric Patients Receiving Intrathecal Nusinersen (SPINRAZA®) for Spinal Muscular Atrophy

Acta cytologica, 2022-01, Vol.66 (1), p.79-84

2022

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2 Genetically distinct Burkitt lymphomas (2 primaries rather than recurrent disease): consider X-linked lymphoproliferative disorder

Journal of pediatric hematology/oncology, 2015-05, Vol.37 (4), p.330-331

Schafernak, Kristian T

2015

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Identification of KMT2A-ARHGEF12 fusion in a child with a high-grade B-cell lymphoma

Cancer genetics, 2021-11, Vol.258-259, p.23-26

2021

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Hermansky‐Pudlak syndrome: Report of two patients with updated genetic classification and management recommendations

Pediatric dermatology, 2017-11, Vol.34 (6), p.638-646

2017

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Rare Presentations of Epstein-Barr Virus–Associated Smooth Muscle Tumor in Children

Pediatric and developmental pathology, 2016-03, Vol.19 (2), p.132-138

2016

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Simultaneous presentation of plasma cell myeloma and acute promyelocytic leukemia

Blood, 2013-12, Vol.122 (24), p.3861-3861

2013

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Pediatric Chronic Myeloid Leukemia Presenting With Extreme Thrombocytosis Simulating Essential Thrombocythemia

Journal of pediatric hematology/oncology, 2018-08, Vol.40 (6), p.456-457

2018

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Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS

Blood advances, 2023-07, Vol.7 (13), p.3307-3311

2023

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Clonality assessment of cutaneous B-cell lymphoid proliferations: a comparison of flow cytometry immunophenotyping, molecular studies, and immunohistochemistry/in situ hybridization and review of the literature

The American journal of dermatopathology, 2014-10, Vol.36 (10), p.781-795

2014

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Classification of Renal Neoplasms Based on Molecular Signatures

The Journal of urology, 2006-06, Vol.175 (6), p.2302-2306

2006

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West Nile virus encephalomyelitis with polio-like paralysis & nigral degeneration

Canadian journal of neurological sciences, 2006-11, Vol.33 (4), p.407-410

2006

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A granulomatous reaction to Avitene mimicking recurrence of a medulloblastoma. Case report

Journal of neurosurgery, 2006-01, Vol.104 (1 Suppl), p.33-36

2006

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Evaluating lymphadenopathy using lymph node FNA

American family physician, 2004-07, Vol.70 (2), p.258-258

Schafernak, Kristian T

2004

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Pediatric renal cell carcinoma as second malignancy: reports of two cases and a review of the literature

Canadian journal of urology, 2007-12, Vol.14 (6), p.3739

2007

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Clinical and Cytogenomic Features of Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21) in the Context of Constitutional Ring Chromosome 21

Blood, 2019-11, Vol.134 (Supplement_1), p.5208-5208

2019

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Reply from the author

Kidney international, 2001-02, Vol.59 (2), p.802-802

Schafernak, Kristian T.

2001

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Hereditary pyropoikilocytosis: a rare but potentially severe form of congenital hemolytic anemia

Journal of pediatric hematology/oncology, 2007-02, Vol.29 (2), p.128-129

2007

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Organ commerce revisited

Kidney international, 2000-08, Vol.58 (2), p.901-901

Schafernak, Kristian T.

2000

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Performance of ACR TI-RADS and the Bethesda System in Predicting Risk of Malignancy in Thyroid Nodules at a Large Children's Hospital and a Comprehensive Review of the Pediatric Literature

Neurogenesis and neuronal differentiation in the postnatal frontal cortex in Down syndrome

Underreporting of perforating osteoma cutis: A call for recognition and diagnostic consistency

Postnatal Cytoarchitecture and Neurochemical Hippocampal Dysfunction in Down Syndrome

Diagnostic work-up of hematological malignancies with underlying germline predisposition disorders (GPD)

Over Expression of Insulin-Like Growth Factor Binding Protein 3 in Clear Cell Renal Cell Carcinoma

High Prevalence of Gene Fusions and Copy Number Alterations in Pediatric Radiation Therapy-Induced Papillary and Follicular Thyroid Carcinomas

Cytochemical Characterization of Cerebrospinal Fluid Macrophage Inclusions in Pediatric Patients Receiving Intrathecal Nusinersen (SPINRAZA®) for Spinal Muscular Atrophy

2 Genetically distinct Burkitt lymphomas (2 primaries rather than recurrent disease): consider X-linked lymphoproliferative disorder

Identification of KMT2A-ARHGEF12 fusion in a child with a high-grade B-cell lymphoma

Hermansky‐Pudlak syndrome: Report of two patients with updated genetic classification and management recommendations

Rare Presentations of Epstein-Barr Virus–Associated Smooth Muscle Tumor in Children

Simultaneous presentation of plasma cell myeloma and acute promyelocytic leukemia

Pediatric Chronic Myeloid Leukemia Presenting With Extreme Thrombocytosis Simulating Essential Thrombocythemia

Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS

Clonality assessment of cutaneous B-cell lymphoid proliferations: a comparison of flow cytometry immunophenotyping, molecular studies, and immunohistochemistry/in situ hybridization and review of the literature

Classification of Renal Neoplasms Based on Molecular Signatures

West Nile virus encephalomyelitis with polio-like paralysis & nigral degeneration

A granulomatous reaction to Avitene mimicking recurrence of a medulloblastoma. Case report

Evaluating lymphadenopathy using lymph node FNA

Pediatric renal cell carcinoma as second malignancy: reports of two cases and a review of the literature

Clinical and Cytogenomic Features of Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21) in the Context of Constitutional Ring Chromosome 21

Reply from the author

Hereditary pyropoikilocytosis: a rare but potentially severe form of congenital hemolytic anemia

Organ commerce revisited

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