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1994 | 1 |
2023 | 1 |
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An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline SDHB pathogenic variant in the absence of paraganglioma or pheochromocytoma.
Front Endocrinol (Lausanne). 2023 Dec 13;14:1273093. doi: 10.3389/fendo.2023.1273093. eCollection 2023.
Front Endocrinol (Lausanne). 2023.
PMID: 38152133
Free PMC article.
However, PAs can be part of a number of familial tumor syndromes such as multiple endocrine neoplasia type 1 (MEN 1) or more rarely in association with pheochromocytoma and PGL (referred to as 3P syndrome). Only a limited number of PAs in association with SDHB-relat …
However, PAs can be part of a number of familial tumor syndromes such as multiple endocrine neoplasia type 1 (MEN 1) or more rarely in assoc …
Molecular genetic analysis of the 3p- syndrome.
Phipps ME, Latif F, Prowse A, Payne SJ, Dietz-Band J, Leversha M, Affara NA, Moore AT, Tolmie J, Schinzel A, et al.
Phipps ME, et al.
Hum Mol Genet. 1994 Jun;3(6):903-8. doi: 10.1093/hmg/3.6.903.
Hum Mol Genet. 1994.
PMID: 7951234
Free article.
Clinical Trial.
Molecular genetic analysis of five cases of 3p- syndrome (del(3)(qter-->p25:)) was performed to investigate the relationship between the molecular pathology and clinical phenotype. ...At least three patients were deleted for the von Hippel-Lindau (VHL) dis …
Molecular genetic analysis of five cases of 3p- syndrome (del(3)(qter-->p25:)) was performed to investigate the relationshi …
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