Results 171 to 180 of about 38,036,070 (284)

The Efficacy of Pharmacotherapy Intervention on Anthropometric Outcomes in Survivors of Childhood Brain Tumors: An Updated Systematic Review and Meta‐Analysis

Obesity Reviews, Volume 27, Issue 10, October 2026.
ABSTRACT Introduction Many survivors of childhood brain tumors face long‐term adverse health outcomes like obesity. Uncertainties surround the effect of interventions to manage obesity‐related outcomes in survivors of childhood brain tumors. The goal of this updated systematic review and meta‐analysis was to provide the best estimate of the treatment ...
David Hart, Lawrence Mbuagbaw, Joseph Beyene, Marwa Akola, Sarah Burrow, M. Constantine Samaan, Lehana Thabane, Adam Fleming, Donna L. Johnston, Shahrad R. Rassekh, Laura Banfield, Russell J. de Souza   +11 more
wiley   +1 more source

Neurofibromatosis type 1

Muller Journal of Medical Sciences and Research, 2013
P Chaitra, M Ramesh Bhat
doaj   +1 more source

Sutural cataract in neurofibromatosis type 1

Indian Journal of Ophthalmology. Case Reports, 2023
Athul S Puthalath, Prashant K Verma, Sreeram Jayaraj   +2 more
doaj   +1 more source

Robotic resection for splenic artery aneurysm associated with neurofibromatosis type 1: a case report

Journal of Medical Case Reports
Background Neurofibromatosis type 1 is an autosomal-dominant disease characterized by café-au-lait spots and neurofibromas, as well as various other symptoms in the bones, eyes, and nervous system.
Akihiko Ueda, Kenta Saito, Hiromichi Murase, Tomokatsu Kato, Hiroyuki Imafuji, Mamoru Morimoto, Ryo Ogawa, Hiroki Takahashi, Yoichi Matsuo, Shuji Takiguchi   +9 more
doaj   +1 more source

A rare case of neurofibromatosis type 1

, 2016
Neurofibromatosis type 1 disease is characterized by pigmented cutaneous lesions and generalized tumors of neural crest origin. Sphenoid dysplasia is one of the characteristics of this syndrome which occurs in 5-10% of the cases.
Vijaya Prasad Balda, Siva Rama Krishna, Satyavaraprasd Kadali   +2 more
core   +1 more source

pathophysiology of neurofibromatosis type 1

Neurofibromatoses are inherited disorders, designated as neurofibromatosis type 1 (NF1), neurofibromatosis type 2, and schwannomatosis, that tend to result in benign tumors of the nerve sheath.
Theos , A.
core  

Neurofibromatosis Type-1 and Hypothyroidism [PDF]

The Indian Journal of Pediatrics, 2020
Prateek Kumar, Panda, Indar Kumar, Sharawat   +1 more
openaire   +2 more sources

Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series

Neurofibromatosis type 1 (NF1) is a multisystemic neurocutaneous disease caused by a heterozygous mutation of the NF1 gene that encodes neurofibromin.
Pruna D., Marica M., Soddu C., Currao P., Savasta S., Satta S., Marras M., Balzarini M., Pavanello M.   +8 more
core   +1 more source

Management of plexiform neurofibromas in neurofibromatosis type 1: An Italian Delphi consensus. [PDF]

Neurol Sci
Santoro C, Arkhangelskaya E, Bonvicino A, Bruno I, Cirillo M, Diana MC, Eoli M, Facchini F, Ionna F, Leoni C, Macchiaiolo M, Marulli G, Nazzi V, Paolini S, Trevisson E, Ruggieri M, Saletti V.   +16 more
europepmc   +1 more source

Cerebellar hemangioblastoma in a patient with neurofibromatosis type 1: A case report. [PDF]

Surg Neurol Int
Stefanoni Galeazzi D, Stefanoni Pérez G.   +1 more
europepmc   +1 more source