[Predicting the presence of <i>MEN1</i> gene mutation based on the clinical phenotype of patients with primary hyperparathyroidism].

Mokrysheva, N G; Eremkina, A K; Miliutina, A P; Salimkhanov, R Kh; Aboishava, L A; Bibik, E E; Gorbacheva, A M; Elfimova, A R; Kovaleva, E V; Popov, S V; Melnichenko, G A

[Predicting the presence of MEN1 gene mutation based on the clinical phenotype of patients with primary hyperparathyroidism].

Mokrysheva, N G; Eremkina, A K; Miliutina, A P; Salimkhanov, R Kh; Aboishava, L A; Bibik, E E; Gorbacheva, A M; Elfimova, A R; Kovaleva, E V; Popov, S V; Melnichenko, G A.

Afiliación

Mokrysheva NG; Endocrinology Research Centre.
Eremkina AK; Endocrinology Research Centre.
Miliutina AP; Endocrinology Research Centre.
Salimkhanov RK; Endocrinology Research Centre.
Aboishava LA; Endocrinology Research Centre.
Bibik EE; Endocrinology Research Centre.
Gorbacheva AM; Endocrinology Research Centre.
Elfimova AR; Endocrinology Research Centre.
Kovaleva EV; Endocrinology Research Centre.
Popov SV; Endocrinology Research Centre.
Melnichenko GA; Endocrinology Research Centre.

Probl Endokrinol (Mosk) ; 69(5): 4-15, 2023 Nov 10.

Article en Ru | MEDLINE | ID: mdl-37968947

Asunto(s)

Hiperparatiroidismo Primario; Neoplasia Endocrina Múltiple Tipo 1; Humanos; Hiperparatiroidismo Primario/genética; Estudios Prospectivos; Neoplasia Endocrina Múltiple Tipo 1/complicaciones; Neoplasia Endocrina Múltiple Tipo 1/genética; Fenotipo; Mutación

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasia Endocrina Múltiple Tipo 1 / Hiperparatiroidismo Primario Límite: Humans Idioma: Ru Revista: Probl Endokrinol (Mosk) Año: 2023 Tipo del documento: Article

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