Results 101 to 110 of about 1,229,635 (199)

Moyamoya syndrome and 6p chromosome rearrangements: Expanding evidences of a new association

, 2016
Background: Moyamoya syndrome represents an etiologically heterogeneous cerebral evolutive angiopathy. It can be associated with both well-characterized and recently described genetic conditions with mendelian inheritance.
D'Avella D, Talenti G, Suppiej A, TENCONI, ROMANO, D'AVELLA, DOMENICO, Morao V, TOLDO, IRENE, Tenconi R, Po' C, Sartori S., Toldo I, SUPPIEJ, AGNESE, MORAO, VERONICA, SARTORI, STEFANO, TALENTI, GIACOMO, CAUSIN, FRANCESCO, PO', CHIARA, Causin F   +17 more
core   +1 more source

Moyamoya syndrome associated with Alagille syndrome: outcome after surgical revascularization.

, 2015
Vasculopathy is well-described in Alagille syndrome (ALGS); however, few data exist regarding neurosurgical interventions. We report 5 children with ALGS with moyamoya who underwent revascularization surgery.
Ichord, Rebecca, Piccoli, David A, Smith, Edward R, Bernard, Timothy J, Spinner, Nancy B, Baird, Lissa C, Kamath, Binita M, Scott, R Michael   +7 more
core   +1 more source

Moyamoya syndrome associated with neurofibromatosis type I in a pediatric patient

São Paulo Medical Journal
CONTEXT: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder among humans. Moyamoya disease is a cerebral vasculopathy that is only rarely observed in association with NF-1, particularly in the pediatric age range ...
Luiz Guilherme Darrigo Júnior, Elvis Terci Valera, André de Aboim Machado, Antonio Carlos dos Santos, Carlos Alberto Scrideli, Luiz Gonzaga Tone   +5 more
doaj   +1 more source

Arterial stroke in a child with Seckel syndrome with a pattern of non‐moyamoya vasculopathy

Clinical Case Reports
Key Clinical Message Seckel syndrome is a rare autosomal recessive disorder, characterized by growth retardation and multiple anomalies associated with CNS vasculopathy.
Samin Alavi, Mitra Khalili, Paniz Mirmoghaddam, Sharareh Kamfar, Negar Shams   +4 more
doaj   +1 more source

Caucasian Familial Moyamoya Syndrome With Rare Multisystemic Malformations

, 2013
Moyamoya disease is an idiopathic progressive steno-occlusive disorder of the intracranial arteries located at the base of the brain. It is associated with the development of compensatory extensive network of fine collaterals.
Nzwalo, H, Gradil, C, Mendonça, C, Vieira, JP, Santos, V   +4 more
core  

Delayed Recognition and Stroke-Predominant Presentation in Down Syndrome-Associated Moyamoya Syndrome. [PDF]

Stroke
Santoro JD, Silverman M, Wang AC, Nagesh D, Ho E, Lucas MC, Otey ST, Yousuf MM, Lee S, Mayne EW, Skotko BG, Steinberg GK, Rafii MS.   +12 more
europepmc   +1 more source

Chinese expert consensus on the treatment and diagnosis of moyamoya disease and moyamoya syndrome (2024). [PDF]

Stroke Vasc Neurol
Ni W, Su J, Fei Y, Gu Y, Mao Y, Wang S, Consensus Expert Committee Members.   +6 more
europepmc   +1 more source

Indirect Bypass With Pericranial Transposition for Moyamoya Syndrome in an Infant. [PDF]

Cureus, 2023
Ajala RT, Nguyen A, Lyon K, Qaiser R.
europepmc   +1 more source

Global burden of moyamoya syndrome in pediatric sickle cell disease and implications for the neurosurgical workforce: a systematic review. [PDF]

Childs Nerv Syst
Haizel-Cobbina J, Heukwa-Tefoung A, Pahari S, Lagunju I, Jordan LC, Aldana P, Dewan MC.   +6 more
europepmc   +1 more source

Recurrent Headaches and Moyamoya Syndrome in a Non-Asian Descendant: A Case Report. [PDF]

Cureus, 2023
Singh A, Patel S, Dudhat A, Bhangu JK, Patil D.   +4 more
europepmc   +1 more source