Margarita Raygada, Ph.D.
Affiliations: | National Institute of Child Health and Human Development, Bethesda, MD, United States |
Website:
http://www.usuhs.mil/mps/grunberg/labalumni.htmlGoogle:
"Margarita Raygada"Mean distance: 16.85 (cluster 29) | S | N | B | C | P |
Parents
Sign in to add mentor| Neil E. Grunberg | grad student | 1986-1992 | Uniformed Services University | |
| (The role of hypothalamic insulin and dopamine in the anorectic effect of cocaine and d-amphetamine) | ||||
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Publications
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| Shetty I, Fuller S, Raygada M, et al. (2020) Adrenocortical carcinoma masquerading as pheochromocytoma: a histopathologic dilemma. Endocrinology, Diabetes & Metabolism Case Reports. 2020 |
| Ilanchezhian M, Fuller SN, Raygada M, et al. (2019) Clinical characterization of patients with SDHC epimutation in gastrointestinal stromal tumors. Journal of Clinical Oncology. 37: 11033-11033 |
| Siegel C, Raygada M, Acquaye A, et al. (2019) RARE-10. IMPROVING CARE FOR ADULT PATIENTS WITH RARE CNS TUMORS: THE NATIONAL CANCER INSTITUTE-COMPREHENSIVE ONCOLOGY NETWORK EVALUATING RARE CNS TUMORS (NCI-CONNECT) PROGRAM AND CLINIC Neuro-Oncology. 21: vi223-vi223 |
| Barakat AJ, Raygada M, Rennert OM. (2018) Barakat syndrome revisited. American Journal of Medical Genetics. Part A |
| Jochmanova I, Wolf KI, King KS, et al. (2017) SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. Journal of Cancer Research and Clinical Oncology |
| Lyssikatos C, Pavithran PV, Tirosh A, et al. (2017) NEWLY DIAGNOSED CARNEY COMPLEX IN 3 YOUNG ADULTS WITH PRIMARY ADRENAL CUSHING SYNDROME – A CASE SERIES AND REVIEW OF THE LITERATURE Aace Clinical Case Reports. 3: e326-e330 |
| Boikos SA, Pappo AS, Killian JK, et al. (2016) Molecular Subtypes of KIT/PDGFRA Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Gastrointestinal Stromal Tumor Clinic. Jama Oncology |
| Nobel YR, Lodish MB, Raygada M, et al. (2016) Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene. Endocrinology, Diabetes & Metabolism Case Reports. 2016: 150104 |
| Schernthaner-Reiter MH, Adams D, Trivellin G, et al. (2016) A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers. European Journal of Pediatrics |
| Boikos SA, Xekouki P, Fumagalli E, et al. (2016) Carney triad can be (rarely) associated with germline succinate dehydrogenase defects. European Journal of Human Genetics : Ejhg. 24: 569-73 |