Results 11 to 20 of about 16,386 (222)

Acquired Chiari Type 1 Malformation Secondary to Paget’s Disease of the Bone: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2021
Chiari type 1 malformations are characterised by caudal descent of cerebellar tonsil into foramen magnum. Usually it is congenital. Paget’s disease causing acquired chiari type 1 malformation is rare with only five reported cases in the literature.
Srestha Khan, Senthil Kumar Aiyappan, Abinesh Govindarajan, Vinayagam Shanmugam   +3 more
doaj   +1 more source

Familial chiari malformation

Journal of Spinal Surgery, 2022
Chiari malformation type 1 (CM 1) is defined asherniation ofcerebellar tonsils 4-5 mm below the foramen magnum. Multiple developmental factors like defective development of pontine flexure and shallow posterior fossa are the proposed factors which ...
Krishnakumar Kesavapisharady, Amjad Mohammed Jamaluddin, Adam Kamrudeen, Tobin George, Ganesh Divakar   +4 more
doaj   +1 more source

Anomalies in the cognitive-executive functions in patients with chiari malformation type I [PDF]

, 2018
Resumen tomado de la publicaciónAnomalías en las funciones cognitivo-ejecutivas en pacientes con la Malformación de Chiari Tipo I. Antecedentes: en la última década, existen evidencias crecientes de que déficits neuropsicológicos, esencialmente en ...
Besteiro González, José Luis, Torres Campa-Santamarina, José María   +1 more
core   +2 more sources

Chiari type I malformation, syncope, headache, hypoglycemia and hepatic steatosis in an 8-year old girl: a causal association?

Pediatric Reports, 2010
Chiari type I malformation (CMI) is a congenital hindbrain anomaly characterized by downward displacement of the cerebellar tonsils through the foramen magnum.
Alberto Spalice, Luigi Tarani, Francesca Del Balzo, Francesco Costantino, Enrico Properzi, Natascia Liberato   +5 more
doaj   +1 more source

Persistent primitive hypoglossal artery associated with Chiari II malformation: Diagnosis and clinical implications

Indian Journal of Radiology and Imaging, 2010
We present a case of persistent primitive hypoglossal artery (PPHA) associated with Chiari II malformation and discuss the clinical implications. There has been one reported case of PPHA associated with Chiari 1 malformation, but none in association with
Mudit Gupta, Rashmi Gupta, Ashu Seith
doaj   +3 more sources

Low-field magnetic resonance imaging and multislice computed tomography for the detection of cervical syringomyelia in dogs [PDF]

, 2015
Background: Syringomyelia (SM) is defined as the presence of fluid- containing cavities within the parenchyma of the spinal cord. Sagittal magnetic resonance (MR) images have been described as the preferred technique for visualizing SMin dogs and humans.
Akiyama, Barone, Bland, Bou-Haider, Brodfelt, Capello, Carruthers, Costa, Couturier, Cross, Dennis, Dewey, Doyon, Drees, Driver, Driver, Feliu-Pascual, Fishbein, Freeman, Greitz, Hecht, Kirberger, Kitagawa, Klekamp, Kromhout, Landis, Lee, Levine, Loderstedt, Olby, Parker, R Core team, Rusbridge, Rusbridge, Rusbridge, Todor, Trigylidas   +36 more
core   +2 more sources

Management and birth outcomes of pregnant women with Chiari malformations : a 14 years retrospective case series [PDF]

, 2018
Objective The management of Chiari malformations in pregnancy is challenging due to the perceived risk of adverse maternal neurological outcomes and raising intracranial pressure during labour.
Al Wattar, Bassel H., Flint, Graham, Pirie, Alex M., Roper, Joanna C., Samarasekera, Shanika, Silva, Adikarige Haritha Dulanka   +5 more
core   +1 more source

Downbeat nystagmus: aetiology and comorbidity in 117 patients [PDF]

, 2008
Objectives: Downbeat nystagmus (DBN) is the most common form of acquired involuntary ocular oscillation overriding fixation. According to previous studies, the cause of DBN is unsolved in up to 44% of cases.
Brandt, Thomas, Glaser, Mirjam, Strupp, Michael, Wagner, Judith N.   +3 more
core   +1 more source

Chiari Type I Malformation Caused by Craniometaphyseal Dysplasia [PDF]

, 2013
Craniometaphyseal dysplasia is a rare genetic condition characterized by progressive thickening of bones in the skull and metaphyseal abnormalities in the long bones.
Arataki, Shinya, Ozaki, Toshifumi, Sugimoto, Yoshihisa, Takigawa, Tomoyuki, Tanaka, Masato, Tetsunaga, Tomoko   +5 more
core   +1 more source

Measures of Health-Related Quality of Life Outcomes in Pediatric Neurosurgery: Literature Review [PDF]

, 2019
Background Improving value in healthcare means optimizing outcomes and minimizing costs. The emerging pay-for-performance era requires understanding of the effect of healthcare services on health-related quality of life (HRQoL).
Desai, Virendra R., Gadgil, Nisha, Lam, Sandi K., Raskin, Jeffrey S., Saad, Shahbaz   +4 more
core   +1 more source