There are no universally accepted diagnostic criteria for large-vessel vasculitides (LVV),
including giant cell arteritis (GCA) and Takayasu arteritis (TAK). Currently, available …

Introduction: Neurofibromatosis type 1 is an autosomal dominant tumour syndrome with an
increased risk of developing central nervous system neoplasms, mostly benign low-grade …

A15-year-old male patient with a known history of neurofibromatosis Type 2 (NF-2)
presented to a tertiary care center with progressive and bilateral vision loss. Clinical …

Abstract Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with
multisystemic involvement, affecting central nervous system, skin, bone system and vessels …

Neurofibromatosis (NF) type 2 is a rare neurological, autosomal dominant and genetic
disorder. It is caused by a mutation in the tumor suppressor gene, called NF2 gene. The …

Although genetic syndromes are often thought of as entities falling under the scope of
pediatrics and pediatric radiology, the sequelae of these conditions frequently extend into …

Нейрофиброматоз-нейрокутанный синдром (синдром с неврологическими и кожными
проявлениями), относится к гетерогенной группе наследственных расстройств …

Magnetic resonance imaging (MRI) is used in the evaluation, diagnosis, and management of
spine-related conditions, eg, degenerative disc disease, cauda equine compression …

533 «Лабораторная диагностика Восточная Европа», 2024, том 13, № 4 и
видоспецифичных праймеров в рамках разработки мультиплексной реал-тайм ПЦР …

This study investigated audiologists' familiarity with Auditory Brainstem Implants (ABIs) in
adult patients with Neurofibromatosis Type 2 (NF2). A secondary purpose of this study was …