Results 141 to 150 of about 44,772 (247)

Giant gluteal and vesical plexiform neurofibromas in a patient with neurofibromatosis type 1: a case report

open access: yesJournal of Medical Case Reports
Background Neurofibromatosis type 1 is a neurocutaneous genetic disorder caused by mutations in the NF1 gene, resulting in the formation of benign tumors called neurofibromas.
Imen Sassi   +4 more
doaj   +1 more source

Neurofibromatosis type 1: Cranial MRI findings [PDF]

open access: yes, 2014
Amaç: Nörofibromatozis tip 1 (NF1, von Recklinghausen hastalığı, periferal nörofibromatozis) öncelikle nöral dokular olmak üzere birçok sistemi tutan nörokutanöz bir hastalıktır.
Sivri, Mesut   +5 more
core  

Neonates born at term with periventricular haemorrhagic infarction: Risk factors and clinical presentation

open access: yesDevelopmental Medicine &Child Neurology, Volume 68, Issue 7, Page 1005-1012, July 2026.
This case series describes infants born near term with periventricular hemorrhagic infarction (PVHI), highlighting seizures as a common early symptom. Neonatal complications during delivery and pro‐thrombotic genetic mutations were slightly more common. MRI‐classified involvement was predominantly in the caudate vein territory.
Aleksandra Zaykova   +6 more
wiley   +1 more source

Walsh & Hoyt: Neurofibromatosis [PDF]

open access: yes, 2005
Clinical and genetic studies had for some time suggested two forms of neurofibromatosis. In 1988, a panel of specialists adopted a classification of the two types. The genes for each form were subsequently cloned. Neurofibromatosis type 1 (NF1), the most
John Kerrison, MD
core  

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

open access: yesJournal of Clinical Periodontology, Volume 53, Issue 7, Page 1068-1099, July 2026.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple   +30 more
wiley   +1 more source

pathophysiology of neurofibromatosis type 1 [PDF]

open access: yes
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 tipo 1 y embarazo: consideraciones sobre un caso clínico Neurofibromatosis type 1 and pregnancy: considerations on a clinical case

open access: yesRevista Médica Electrónica, 2012
Se presenta el caso de gestante de 27 años de edad, afecta de neurofibromatosis tipo 1, diagnosticada preconcepcionalmente, la cual fue atendida en el consultorio del médico de familia no.
Pedro Lorenzo Rodríguez Domínguez   +1 more
doaj  

Healthcare utilization patterns and costs related to neurofibromatosis 1 in Ontario, Canada. [PDF]

open access: yesOrphanet J Rare Dis
Sivadasan A   +6 more
europepmc   +1 more source

Gender response to neurofibromatosis 1 [PDF]

open access: yes
This paper explores differing patterns of gender response to neurofibromatosis 1 (NF1), a neurological genetic disorder. Perceptions of gender response expressed by persons with the condition and research findings about lifestyle and attitudinal ...
Ablon, Joan
core  

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