المؤلفون: Tatiana S. Belysheva, Tatiana V. Nasedkina, Timur T. Valiev, Elena V. Sharapova, Vera V. Semenova, Valentina M. Kozlova, Svetlana N. Mikhaylova, Irina S. Kletskaya, Alexey V. Butuzov, Yana V. Vishnevskaja, Valeria V. Lozovaya, Olga A. Gusarova, Armen O. Tumanyan, Olga A. Malichova, Svetlana R. Varfolomeeva

المصدر: Вопросы современной педиатрии, Vol 22, Iss 4, Pp 331-342 (2023)

مصطلحات موضوعية: hereditary polyposis syndromes, hamartomatous polyposis, adenomatous polyposis, peutz-jeghers syndrome, cowden syndrome, hereditary juvenile polyposis, familial adenomatous polyposis, mutyh-associated polyposis, lynch syndrome, endoscopic examination, endoscopic treatment, polypectomy, colorectal cancer, gene mutation, apc, mutyh, stk11, smad4, bmpr1a, pten, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://vsp.spr-journal.ru/jour/article/view/3271; https://doaj.org/toc/1682-5527; https://doaj.org/toc/1682-5535

URL الوصول: https://doaj.org/article/011e6e7a0dea4c1fbb5c37943a6d301f

المؤلفون: Vladimir G. Polyakov, Ruslan V. Shishkov, Aleksei A. Ilyin, Severskaya N. Viktorovna, Natalia V. Ivanova, Roman I. Pimenov, Valentina M. Kozlova, Faina A. Amosenko, Ludmila N. Lubchenko, Tatyiana P. Kazubskaya, Alentina I. Pavlovskaya, Oleg P. Bleznukov, Natalia A. Koshechkina, Elena V. Mikhaylova, Tamara R. Panferova, Irina I. Matveeva, Irina N. Serebryakova, Svetlana N. Mikhaylova, Victor S. Medvedev, Pavel A. Isaev, Pavel O. Rumyantsev, Alexandr U. Abrosimov, Natalia U. Kalinchenko

المصدر: Клиническая и экспериментальная тиреоидология, Vol 12, Iss 1, Pp 22-33 (2016)

مصطلحات موضوعية: preventive thyroidectomy, hereditary medullary thyroid cancer, syndrome of multiple endocrine disorders 2a type (men2a), ret gene germline mutation, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://cet-endojournals.ru/ket/article/viewFile/7867/5826; https://doaj.org/toc/1995-5472; https://doaj.org/toc/2310-3787

URL الوصول: https://doaj.org/article/90e86b64155241c3acf2c2b1131c150e

المؤلفون: Pavel O. Rumyantsev, Alentina I. Pavlovskaya, V. Kozlova, Elena V. Mikhaylova, Natalia U. Kalinchenko, Oleg P. Bleznukov, Natalia V. Ivanova, Irina I. Matveeva, Irina N. Serebryakova, Tatyiana P. Kazubskaya, Alexandr U. Abrosimov, V.G. Polyakov, Faina A. Amosenko, Victor S. Medvedev, P. A. Isaev, Ludmila N. Lubchenko, Severskaya N. Viktorovna, Svetlana N. Mikhaylova, Natalia A. Koshechkina, Ruslan V. Shishkov, Tamara R. Panferova, R. I. Pimenov, Aleksei A. Ilyin

المصدر: Клиническая и экспериментальная тиреоидология, Vol 12, Iss 1, Pp 22-33 (2016)

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Pathology, endocrine system diseases, syndrome of multiple endocrine disorders 2a type (men2a), 030209 endocrinology & metabolism, ret gene germline mutation, Diseases of the endocrine glands. Clinical endocrinology, Pheochromocytoma, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Internal medicine, medicine, hereditary medullary thyroid cancer, Lymph node, business.industry, Thyroid, Medullary thyroid cancer, Cancer, General Medicine, medicine.disease, RC648-665, Dissection, medicine.anatomical_structure, preventive thyroidectomy, 030220 oncology & carcinogenesis, business, Asymptomatic carrier

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958cbd9efc06843e915abbf8c972001d
https://cet-endojournals.ru/ket/article/viewFile/7867/5826