Results 61 to 70 of about 66,319 (312)

Do the cervical spinal canal dimensions predict pre-myelopathic changes of cervical spinal cord? - a magnetic resonance image study

open access: yesNational Journal of Clinical Anatomy, 2015
Background and aims: The cervical region is the most mobile portion of the spinal column and it is here that the earliest disc degenerations are encountered. Hence it is of great interest to neurologists and neurosurgeons.
Smitha S Nair   +3 more
doaj   +1 more source

Further Evidence That Chondrocalcinosis 1 (CCAL1) is a Confirmed Mendelian Phenotype With a Known Molecular Basis

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Chondrocalcinosis (CCAL), also known as calcium pyrophosphate dihydrate deposition disease (CPPDD), is a frequent multifactorial condition in the elderly, but there are two rare autosomal dominant Mendelian forms, CCAL1 (OMIM %600668) and CCAL2. Only three families with molecularly proven CCAL1 have been reported.
Anna‐Christina Pansa   +4 more
wiley   +1 more source

Cervical spinal canal narrowing and cervical neurologi-cal injuries

open access: yesChinese Journal of Traumatology, 2012
【Abstract】Cervical spinal canal narrowing can lead to injury of the spinal cord and neurological symptoms in-cluding neck pain, headache, weakness and parasthesisas.
ZHANG Ling   +5 more
doaj  

Whole spinal pneumorrhachis following perforation of the rectum: A case report

open access: yesRadiology Case Reports
Spinal pneumorrhachis is a relatively rare condition. Herein, we describe a case of whole spinal pneumorrhachis. A 68-year-old male, with a history of total proctocolectomy due to ulcerative colitis, had fever, diarrhea, and inflammatory reactions ...
Hiroshi Kageyama, MD, PhD
doaj   +1 more source

Expanding the Clinical Spectrum of Cousin Syndrome: A Novel Biallelic Missense Variant in TBX15 Causing a Milder Phenotype

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cousin syndrome is a rare skeletal dysplasia characterized by distinctive facial features, humeroradial synostosis, and hypoplasia of the ilia and scapula. Since the original description of the phenotype in two cases by Cousin in 1982, only three additional cases have been published.
Suzanne E. L. Detiger   +3 more
wiley   +1 more source

RIB PENETRATION INTO THE SPINAL CANAL IN CASES OF SCOLIOSIS IN PATIENTS WITH NEUROFIBROMATOSIS TYPE-1 (case report and literature review)

open access: yesTravmatologiâ i Ortopediâ Rossii, 2017
Background. Rib penetration into the spinal canal in patients with scoliosis secondary to neurofibromatosis type-1 (NF-1) was described in a relatively small number of publications, though it’s common in clinical practice and not always diagnosed ...
M. V. Mikhaylovsky   +3 more
doaj   +1 more source

TARDBP (TDP‐43) Knock‐in Zebrafish Display a Late‐Onset Motor Phenotype and Loss of Large Spinal Cord Motor Neurons

open access: yesAnnals of Neurology, EarlyView.
Objective Mutations in TARDBP (encoding TDP‐43) are associated with the neurodegenerative disease amyotrophic lateral sclerosis (ALS) and include familial missense mutations where there are a lack of models and mechanisms examining how they are pathogenic.
Ziyaan A. Harji   +10 more
wiley   +1 more source

Atlantoaxial dislocation in an adolescent with juvenile spondyloarthritis

open access: yesХирургия позвоночника, 2019
Atlantoaxial dislocation with spinal canal stenosis not associated with craniovertebral junction malformations and traumatic injury is a rare pathology in children and adolescents. A clinical case of the diagnosis and surgical treatment of atlantoaxial
Sergei V. Vissarionov   +2 more
doaj   +1 more source

Early synapsids neurosensory diversity revealed by CT and synchrotron scanning

open access: yesThe Anatomical Record, EarlyView.
Abstract Non‐mammaliaform synapsids (NMS) represent the closest relatives of today's mammals among the early amniotes. Exploring their brain and nervous system is key to understanding how mammals evolved. Here, using CT and Synchrotron scanning, we document for the first time three extreme cases of neurosensory and behavioral adaptations that probe ...
J. Benoit   +6 more
wiley   +1 more source

Congenital narrowing of the spinal canal [PDF]

open access: yesSpinal Cord, 1967
Further examples of congenital narrowing of the spinal canal in the lumbar and cervical regions are presented. It is implied that the condition is a nosological entity. Neurogenic intermittent claudication often accompanies the lumbar variety; the diagnosis in the cervical region is, however, radiological.
openaire   +3 more sources

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