Results 181 to 190 of about 38,029,237 (226)

Genotype-negative multiple endocrine neoplasia type 1 with prolactinoma, hyperparathyroidism, and subclinical Cushing's syndrome accompanied by hyperglycemia: a case report. [PDF]

Front Endocrinol (Lausanne)
Kubo H, Wada R, Sekikawa N, Nomura Y, Yamada M, Inoue M, Hattori N, Yamazaki Y, Sugimoto K.   +8 more
europepmc   +1 more source

Role of Nutrition in the Management of Patients with Multiple Endocrine Neoplasia Type 1. [PDF]

Nutrients
Marinari M, Marini F, Giusti F, Brandi ML.   +3 more
europepmc   +1 more source

Multiple endocrine neoplasia type 1

Seminars in Cancer Biology, 2000
The recent cloning of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1) has opened new avenues for both clinical and basic science research in the field of endocrine oncology. A large amount of genetic information, particularly those in relation to germline and somatic mutations, has since been published during the last 2 years. This
F, Ki Wong, J, Burgess, M, Nordenskjöld, C, Larsson, B, Tean Teh   +4 more
core   +6 more sources

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MULTIPLE ENDOCRINE NEOPLASIA TYPE 1 AND ADRENAL LESIONS

Journal of Urology, 2001
We investigated the relationship of long-term pancreatic hormone hypersecretion with adrenal lesions in patients with multiple endocrine neoplasia type 1 and in those with sporadic pancreatic endocrine tumors.We assessed the prevalence of adrenal lesions in 20 patients with multiple endocrine neoplasia type 1 and in a control group of 12 with sporadic ...
Francesco Fallo, Marco Boscaro
exaly   +4 more sources

Genetics of Multiple Endocrine Neoplasia Type 1/Multiple Endocrine Neoplasia Type 2 Syndromes

Endocrinology and Metabolism Clinics of North America, 2017
Multiple endocrine neoplasia syndromes types 1 and 2 represent well-characterized yet clinically heterogeneous hereditary conditions for which diagnostic and management recommendations exist; genetic testing for these inherited endocrinopathies is included in these guidelines and is an important part of identifying affected patients and their family ...
Gilbert Coté
exaly   +3 more sources