Results 101 to 110 of about 16,386 (222)

Preoperative radiological and electrophysiological evaluation in 100 adolescent idiopathic scoliosis patients [PDF]

, 2018
This is a prospective study of spinal magnetic resonance imaging (MRI), electrophysiological recordings, and neurological examinations of 100 patients admitted for surgery for adolescent idiopathic scoliosis (AIS), which was conducted to assess the ...
Böni, Thomas, Curt, Armin, Hausmann, Oliver, Min, Kan, Pfirrmann, Christian   +4 more
core  

Post-infarct cerebellar cognitive affective syndrome: a case report [PDF]

, 2008
Post Infarct cerebellar cognitive affective syndrome is a rare disorder, characterized by cognitive impairment in the domains of memory, language, visuo-spatial functioning and affect after cerebellar stroke.
Jawaid, Ali, Khealani, Bhojo A, Rauf, Muhammad Ameen, Usman, Uzma   +3 more
core   +1 more source

Determination of Clinical Outcome of Surgery in Patients with Chiari 1 Malformation

Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2011
BACKGROUND AND OBJECTIVE: Chiari 1 malformation is a congenital anomaly defined as downward displacement of cerebellar tonsils through the foramen magnum. Various surgical procedures have been presented for this malformation with diverse results. In this
SGA Jorsaraei
doaj  

A Closer Look at the Global Management of Spina Bifida: The Implementation of Endoscopic Third Ventriculostomy in the Treatment of Spina Bifida-Related Hydrocephalus in Africa [PDF]

, 2018
Spina bifida, specifically myelomeningocele, is a debilitating neural tube defect that affects patients and families throughout the world. Traditional management and treatment methods are described, followed by an explanation of why this is often ...
Burckart, Caryssa
core   +1 more source

Chromosomal map of human brain malformations [PDF]

, 2018
The etiology of most central nervous system (CNS) malformations remains unknown. We have utilized the fact that autosomal chromosome aberrations are commonly associated with CNS malformations to identify new causative gene loci.
Lurie, Iosif, Schinzel, Albert, Tyshchenko, Nataliya   +2 more
core  

Surgical Management of Chiari Malformation Type I in the Pediatric Patients with Syringomyelia and Related to Klippel-Feil Syndrome: A Case Series and Literature Review

Acta Medica Bulgarica
Chiari type I malformation (CM-1) is a birth defect where the back part of the skull does not develop properly, leading to the formation of a small and shallow space at the back of the head.
Encarnacion-Santos D. A., Chmutin G., Anvardzhonovich I. B., Chmutin E., Arstanbekov B., Kurbonov Sh., Bodanova S., Chaurasia B.   +7 more
doaj   +1 more source

Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management [PDF]

, 2010
Thomas H. Milhorat, Misao Nishikawa, Roger W. Kula, Yosef D. Dlugacz   +3 more
core   +1 more source

Brain and ventricular volume in patients with syndromic and complex craniosynostosis [PDF]

, 2011
T. de Jong, B. F. M. Rijken, M. H. Lequin, M. L. C. van Veelen, I. M. J. Mathijssen   +4 more
core   +1 more source

[Chiari malformation].

Boletin medico del Hospital Infantil de Mexico, 1991
The Chiari malformation (CHM) is a congenital disease of unknown etiology. It is presumed that a defective closure of the neural tube produces at least one of its three types. It has also been related to traumatic delivery. Type II is closely associated to the myelomeningocele.
J A, Lazareff, P, Valencia-Mayoral
openaire   +1 more source

Chiari malformation type I with cervicothoracic syringomyelia masquerading as bibrachial amyotrophy: a case report [PDF]

, 2015

core   +1 more source