Shing Oh, K., Alloush, F., ..., Brathwaite, C. (2023). FANCC and PTCH1 gene loss in congenital infantile rhabdomyosarcoma with spindle cell features.
Pediatric blood & cancer,
70(4), e30083.
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Oh, K.S., Bahmad, H.F., ..., Brathwaite, C. (2023). Recurrent PIK3CA H1047R-Mutated Congenital Infiltrative Facial Lipomatosis: A Case Report and Review of Literature.
Current issues in molecular biology,
45(2), 1712-1719.
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Fayiga, F.F., Reyes-Hadsall, S.C., ..., Brathwaite, C. et al (2023). Novel ANKRD26 and PDGFRB gene mutations in pediatric case of non-Langerhans cell histiocytosis: Case report and literature review.
Journal of cutaneous pathology,
50(5), 425-429.
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Majluta Yeb, A., Dedic, E., ..., Brathwaite, C. et al (2023). Leukocytoclastic Vasculitis in an Adolescent with New-Onset Crohn's Disease.
JPGN reports,
4(4), e359.
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Baboun, D., Solano, N., ..., Brathwaite, C., et al (2023). Malignancy Risk in Nodules Classified as Atypia of Undetermined Significance in a Predominantly Hispanic Free-Standing Children’s Hospital?.
Journal of the Endocrine Society,
7(Supp 1), A786.
Martinez-Sanchez, A., Baboun, D., ..., Brathwaite, C., et al (2023). Molecular Makeup of Differentiated Thyroid Carcinoma in a Free-Standing Children’s Hospital with a Predominantly Hispanic Population.
Journal of the Endocrine Society,
7(Supp 1), A786-A787.
Palacio-Uribe, L., Perez-Roman, R.J., ..., Brathwaite, C., et al (2022). Cervical intramedullary teratoma: a case report and systematic review of the literature.
Child's nervous system,
38(5), 997-1004.
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Bahmad, H.F., Gogola, S., ..., Brathwaite, C., et al (2022). Hemophagocytic Lymphohistiocytosis in the Setting of Therapy-Induced Acute Myeloid Leukemia: An Autopsy Report.
Diseases,
10(3), 54.
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Bahmad, H.F., Ramesar, L., ..., Brathwaite, C., et al (2022). Histopathologic Findings Associated with Miller-Dieker Syndrome: An Autopsy Report
.
Diseases,
10(4), 95.
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Shing Oh, K., Bahmad, H.F., Brathwaite, C., et al (2021). Neonatal acute liver failure with pulmonary yellow hyaline membrane and kernicterus.
Autopsy & case reports,
11(), e2021268.
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Gupta, R., Calixto-Hope, G.L., ..., Brathwaite, C., et al (2021). Low-grade glioneuronal tumors with FGFR2 fusion resolve into a single epigenetic group corresponding to 'Polymorphous low-grade neuroepithelial tumor of the young'.
Acta neuropathologica,
142(3), 595-599.
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Roberts, A.G., Bujarska, M., ..., Brathwaite, C., et al (2021). Gastric Adenocarcinoma and Proximal Polyposis of the Stomach in a Hispanic Pediatric Patient With APC Gene Variant c.-191T>G.
JPGN reports,
2(4), e123.
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Mondal, G., Lee, J.C., ..., Brathwaite, C., et al (2020). Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition.
Acta neuropathologica,
139(6), 1071-1088.
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Goyal, A., Cajigas, I., Ibrahim, G.M., Brathwaite, C.D., Khatib, Z., et al (2018). Surgical Treatment of Intramedullary Spinal Metastasis in Medulloblastoma: Case Report and Review of the Literature.
World neurosurgery,
118(), 42-46.
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Chim, H., Al-Qattan, H., Valencia, H., Brathwaite, C., Price, A., Grossman,J.A. (2017). Intravenous Glomus Tumor Masquerading as Lateral Antebrachial Cutaneous Neuroma.
Hand (NY),
12(2), NP19-NP21.
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Huse, J.T., Snuderl, M., Jones, D.T., Brathwaite, C.D., Altman, N., Lavi, E., Saffery, R., et al (2017). Polymorphous low-grade neuroepithelial tumor of the young (PLNTY): an epileptogenic neoplasm with oligodendroglioma-like components, aberrant CD34 expression, and genetic alterations involving the MAP kinase pathway.
Acta Neuropathologica,
133(3), 417-429.
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Pichardo, C., Muinos, W., Brathwaite, C., Hernandez, E. (2017). Pulmonary Hemosiderosis Associated With Celiac Disease: Lane Hamilton Syndrome.
Journal of Pediatric Gastroenterology and Nutrition,
64(5), e133.
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Satahoo, S.S., Brathwaite, C., Davis, J.S., Burnweit, C. (2013). Obstructing apple core lesion of the rectum: a case report of inflammatory pseudotumor masquerading as colorectal carcinoma.
Journal of Pediatric Surgery,
48(3), 677-680.
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Alrazzak, M.A., Brathwaite, C.D., Restrepo, R., Khatib, Z.A. (2013). Plasma Cell Granuloma of the Lung in the Differential Diagnosis of Pulmonary Nodules in a Child with Acute Lymphoblastic Leukemia.
The Internet Journal of Oncology,
9(1), .
http://ispub.com/IJO/9/1
Vrotsos, E., Soaita, M., Khatib, Z.A., Brathwaite, C.D., Filipovich, A., Robinson, M.J., Castellano-Sanchez, A. (2012). Atypical clinical presentation of primary hemophagocytic lymphohistiocytosis with a novel perforin1 gene mutation.
Journal of Hematopathology,
http://link.springer.com/journal/12308
Alghamdi, S., Castellano-Sanchez, A., Brathwaite, C., Shimizu, T., Khatib, Z., Bhatia, S. (2012). Strong desmin expression in a congenital desmoplastic infantile ganglioglioma mimicking pleomorphic rhadomyosarcoma: a case report including ultrastructural and cytogenetic evaluation and review of the literature.
Child's Nervous System,
28(12), 2157-2162.
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Kram, D.E., Brathwaite, C.D., Khatib, Z.A. (2010). Bilateral conjunctival extranodal marginal zone B-cell lymphoma.
Pediatric Blood & Cancer,
55(7), 1414-1416.
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Zoeller, G.K., Brathwaite, C.D., Sandberg, D.I. (2010). Malignant transformation of an optic pathway glioma without prior radiation therapy.
Journal of Neurosurgery. Pediatrics,
5(5), 507-510.
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Covington, D.B., Rosenblum, M.K., Brathwaite, C.D., Sandberg, D.I. (2009). Angiocentric glioma-like tumor of the midbrain.
Pediatric Neurosurgery,
45(6), 429-433.
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Gupta, P., Goyal, S., Gonzalez-Mendoza, L.E., Noviski, N., Vemar, M., Brathwaite, C.D., Misra, M. (2008). Corticotropin-independent cushing syndrome in a child with an ovarian tumor misdiagnosed as nonclassic congenital adrenal hyperplasia.
Endocrine Practice,
14(7), 875-879.
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Wykoff, C. C., Lam, B. L., Brathwaite, C. D., Biegel, J. A., McKeown, C. A., Rosenblum, M.K., Allewelt, H.B., Sandberg, D.I. (2008). Atypical teratoid/rhabdoid tumor arising from the third cranial nerve.
Journal of Neuro-Ophthalmology,
28(3), 207-211.
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