НОВЫЙ ВЗГЛЯД НА БОЛЕЗНЬ РЕКЛИНГХАУЗЕНА (НЕЙРОФИБРОМАТОЗ 1 ТИПА) of tumors in humans -
neurofibromatosis type 1, belonging to the group of phacomatosis. Patient observations
Skeletal anomalies in patients with neurofibromatosis type 1Introduction
Neurofibromatosis type 1 (NF1) is one of the most common hereditary tumor syndromes
Immune system changes in the pathogenesis of neurofibromatosis type 1Neurofibromatosis type 1 (NF1) is a hereditary tumor syndrome occurring with a frequency of 1: 3000
Prospects for the use of statins in the treatment of neurofibromatosis type 1Prospects for the use of statins in the treatment of
neurofibromatosis type 1
Prospects for the treatment of neurofibromatosis type 1: A reviewNeurofibromatosis type 1 (NF1) is an autosomal dominant hereditary tumor syndrome with a prevalence
PROSPECTS FOR DIAGNOSTICS AND TREATMENT OF NEUROFIBROMATOSIS TYPE 1 IN RUSSIAPROSPECTS FOR DIAGNOSTICS AND TREATMENT OF
NEUROFIBROMATOSIS TYPE 1 IN RUSSIA
Neurofibromatosis type 1: Results of our own study (Republic of Bashkortostan)Mustafin, R.N.,
Bermisheva, M.A.,
Valiev, R.R.,
Khusnutdinova, E.K.,
Мустафин, Р. Н.,
Бермишева, М. А.,
Валиев, Р. Р.,
Хуснутдинова, Э. К. Neurofibromatosis type 1: Results of our own study (Republic of Bashkortostan)
ATYPICAL CLINICAL MANIFESTATIONS AND GENOTYPE-PHENOTYPE CORRELATIONS OF NEUROFIBROMATOSIS TYPE 1 of
neurofibromatosis type 1. Material and Methods. We searched for relevant sources in the Scopus, Web of Science, Pub