Results 91 to 100 of about 27,985,342 (173)

Chiari I Malformation Associated with Turner Syndrome

open access: yes, 2017
Turner syndrome (TS) is a rare genetic disease due to the absence of one X chromosome. Patients with TS have more subtle neurological/neuropsychiatric problems, while headache is an uncommon clinical presentation which needs attention.
Jeevan S. Nair   +1 more
core   +1 more source

Chiari type I malformation in children

open access: yes, 2011
The diagnosis of Chiari type I malformation (CIM) is more and more frequent in clinical practice due to the wide diffusion of magnetic resonance imaging. In many cases, such a diagnosis is made incidentally in asymptomatic patients, as including children
Massimi, Luca   +5 more
core   +1 more source

MALFORMAÇÃO DE CHIARI I: RELATO DE CASO

open access: yesRevista Uningá, 2019
RESUMO Introdução: A Malformação de Chiari tipo I é uma alteração congênita e pouco prevalente que é originária de anomalias estruturais da base do crânio com uma fossa craniana posterior hipoplásica que leva à herniação das tonsilas cerebelares pelo
Illgner Alves de Souza   +4 more
doaj  

The importance of precise plane selection for female adult Chiari Type I malformation midsagittal morphometrics. [PDF]

open access: yesPLoS One, 2022
Morkos M   +7 more
europepmc   +1 more source

Chiari I Malformation Associated With Callosal Dysgenesis and Ectopic Neurohypophysis

open access: yes, 1995
In patients with Chiari I malformation there usually is no anomaly of the supratentorial structures. In this communication we report a patient with Chiari I malformation, callosal dysgenesis, and an ectopic neurohypophysis.
Sener, RN, R.Nuri Sener
core   +1 more source

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