نتائج البحث

Giant prolactinoma, germline BRCA1 mutation, and depression: a case report

• Authors : Rita Bettencourt-Silva; Joana Queirós; Josué Pereira

Subjects: Prolactinoma; Prolactin; BRCA

• Source: Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-7 (2018)

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Giant prolactinoma, germline BRCA1 mutation, and depression: a case report.

• Authors : Bettencourt-Silva R; Department of Endocrinology, Diabetes and Metabolism, Centro Hospitalar Universitário de São João, E.P.E., Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal. .; Faculty of Medicine, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal. .

Subjects: BRCA1 Protein/BRCA1 Protein/BRCA1 Protein/*genetics ; Depressive Disorder/Depressive Disorder/Depressive Disorder/*complications ; Mutation/Mutation/Mutation/*genetics

• Source: Journal of medical case reports [J Med Case Rep] 2018 Dec 06; Vol. 12 (1), pp. 360. Date of Electronic Publication: 2018 Dec 06.Publisher: BioMed Central Country of Publication: England NLM ID: 101293382 Publication Model: Electronic Cited Medium: Internet ISSN: 1752-1947

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A novel PTCH1 germline mutation distinguishes basal cell carcinoma from basaloid follicular hamartoma: a case report

• Authors : Hellani Ali; Baghdadi Hiba; Dabbour Nidal

Subjects: Medicine

• Source: Journal of Medical Case Reports, Vol 3, Iss 1, p 52 (2009)

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Somatic PRKAR1A mutation in sporadic atrial myxoma with cerebral parenchymal metastases: a case report

• Authors : Jeffrey Sklar; Joachim M. Baehring; Jennifer Adams

Subjects: Pathology; medicine.medical_specialty; PRKAR1A mutation

• Source: Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-9 (2019)Journal of Medical Case Reports

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Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports

• Authors : Kazuhiro Takekoshi; Tetsuo Nishikawa; Naoki Hasegawa

Subjects: Adult; 0301 basic medicine; endocrine system diseases

• Source: Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)Journal of Medical Case Reports

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Familial adenomatous polyposis: a case report.

• Authors : Kindie, Endeshaw Asaye¹ (AUTHOR) ; Beyera, Tigist Desta² (AUTHOR); Teferi, Ephrem Tafesse¹ (AUTHOR)

• Source: Journal of Medical Case Reports. 9/8/2024, Vol. 18 Issue 1, p1-9. 9p.

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Rectal leiomyosarcoma as the initial phenotypic manifestation of Li–Fraumeni-like syndrome: a case report and review of the literature.

• Authors : Severino, Natalia Parisi¹ (AUTHOR) ; Waisberg, Jaques^2,3 (AUTHOR); Fragoso, Maria Candida Barisson Villares⁴ (AUTHOR)

• Source: Journal of Medical Case Reports. 12/19/2022, Vol. 16 Issue 1, p1-7. 7p.

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Challenges in the management of metastatic gastrointestinal stromal tumor in a patient with neurofibromatosis type 1: a case report.

• Authors : Bharath, B. G.¹ (AUTHOR); Rastogi, Sameer¹ (AUTHOR) ; Ahmed, Shamim² (AUTHOR)

• Source: Journal of Medical Case Reports. 5/1/2022, Vol. 16 Issue 1, p1-7. 7p.

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Malignant phyllodes tumor in Lynch syndrome: a case report

• Authors : Rebecca C. Heintzelman; Shayma Kazmi; Melanie Corbman

Subjects: Oncology; Adult; medicine.medical_specialty

• Source: Journal of Medical Case ReportsJournal of Medical Case Reports, Vol 13, Iss 1, Pp 1-7 (2019)

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Hereditary breast and ovarian cancer triggered by occult fallopian tube cancer: a case report.

• Authors : Murakami, Hikaru¹ (AUTHOR); Fujiwara, Satoe¹ (AUTHOR) ; Nishie, Ruri¹ (AUTHOR)

• Source: Journal of Medical Case Reports. 8/18/2023, Vol. 17 Issue 1, p1-6. 6p.

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