Results 61 to 70 of about 5,376 (172)
Osteopetrosis and Chiari type I malformation: a rare association [PDF]
Journal of Surgical Case Reports, 2015 Osteopetrosis (OP) is hereditary X-linked, autosomal recessive (ARO), or autosomal dominant (ADO) skeletal disease. ARO has two subtypes, which are infantile malignant and intermediate type. ARO and X-linked OP have poor clinical outcome. ADO is called adult benign type because of the normal life expectancy, which has type I and type II.
Ekici, Mehmet Ali +3 more
openaire +2 more sources
Outcomes of 87 small‐breed dogs surgically treated for Chiari‐like malformation and syringomyelia
Veterinary Surgery, EarlyView.Abstract Objective To report the outcomes of titanium mesh (TM) cranioplasty without polymethylmethacrylate (PMMA), incorporating a deliberate gap between the foramen magnum decompression (FMD) surface and the TM, in small‐breed dogs with Chiari‐like malformation and syringomyelia (CM/SM). Study design Retrospective clinical study.
Sung Su Park, Ji Young Park, Ho Jae Han
wiley +1 more source
Case Reports in Anesthesiology, 2013 Anesthetic management of laboring parturients with Arnold-Chiari type I malformation poses a difficult challenge for the anesthesiologist. The increase in intracranial pressure during uterine contractions, coughing, valsalva maneuvers, and expulsion of ...
Clark K. Choi, Kalpana Tyagaraj
doaj +1 more source
Experimental Physiology, EarlyView.Abstract Modulation of bone marrow adipose tissue (BMAT) with prolonged inactivity was reported in haemopoietic but not in non‐haemopoietic bones. This prospective randomized controlled trial submitted 16 men and 8 women to 60 days of 6° head‐down‐tilt bed rest.
Tammy Liu +5 more
wiley +1 more source
A star in the daylight clinical vignette: Lesional focal epilepsy with cerebral accessory falx
Epileptic Disorders, EarlyView.
Kyle McGrath +3 more
wiley +1 more source
Controversies Surrounding Critical‐Size Defects: Influence of Age and Biological Characteristics
Journal of Biomedical Materials Research Part B: Applied Biomaterials, Volume 114, Issue 6, June 2026.ABSTRACT Critical‐size defects (CSDs) in craniofacial reconstruction refer to osseous gaps that fail to heal spontaneously, increasing the risk of neurological impairment and craniofacial dysmorphology. Despite decades of investigation, controversy still exists surrounding the definition of CSDs, with criteria varying across species, experimental ...
Andrew Nordlund +7 more
wiley +1 more source
Acta Medica BulgaricaChiari 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. +7 more
doaj +1 more source
Chiari type I and II malformations
South African Journal of Radiology, 2002 No abstract available.
S. Andronikou, C. Welman, E. Kader
openaire +3 more sources
Analysis of Visuospatial Abilities in Chiari Malformation Type I
The Cerebellum, 2019 The involvement of the cerebellum in visuospatial abilities has been evidenced in numerous studies, based on the cerebellar-cortical circuitry. This domain has been evaluated in several patients with cerebellar disorders, but the assessment of visuospatial processing in Chiari malformation type I (CM-I) is scarce.
Maitane García +8 more
openaire +2 more sources
Late otoneurologic manifestations of Chiari I malformation
International Archives of Otorhinolaryngology, 2011 Introduction: Chiari malformation (CM) belongs to an anomaly group comprised of the structures in the cranial-cerebellar-medullary junctions. Type I (CM I) is characterized by the descent of the cerebellar tonsils and the medial portion of the lower ...
Oliveira, Neide Fátima Cordeiro Diniz +2 more
doaj