Results 121 to 130 of about 3,460 (171)
Some of the next articles are maybe not open access.
Pediatric Neurosurgery, 2010
<i>Objective:</i> Cervical spinal dysraphism is a rare congenital spinal pathology. The results obtained from our series are compared with the results obtained from other series of studies in the literature. <i>Methods:</i> Seven patients with cervical myelomeningocele and meningocele who underwent surgery between January 1996 ...
Kozan, Abdulbaki +4 more
openaire +3 more sources
<i>Objective:</i> Cervical spinal dysraphism is a rare congenital spinal pathology. The results obtained from our series are compared with the results obtained from other series of studies in the literature. <i>Methods:</i> Seven patients with cervical myelomeningocele and meningocele who underwent surgery between January 1996 ...
Kozan, Abdulbaki +4 more
openaire +3 more sources
Spinal Dysraphism in Achondroplasia
Pediatric Neurosurgery, 2008The neurological complications in achondroplasia are commonly due to spinal canal stenosis. A case with rare coexistence of achondroplasia and dysraphic condition of the spine is presented wherein the neurological problem was presumably due to the latter.
R V, Phadke +2 more
openaire +2 more sources
Pediatrics In Review, 2019
1. Lucy C. Holmes, MD, MPH*,‡ 2. Veetai Li, MD†,‡ 1. *Department of Pediatrics, 2. †Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY 3. ‡John R. Oishei Children’s Hospital, Buffalo, NY Spinal dysraphism is an incomplete fusion of the spine during embryologic development and encompasses a spectrum ...
Lucy C, Holmes, Veetai, Li
openaire +2 more sources
1. Lucy C. Holmes, MD, MPH*,‡ 2. Veetai Li, MD†,‡ 1. *Department of Pediatrics, 2. †Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY 3. ‡John R. Oishei Children’s Hospital, Buffalo, NY Spinal dysraphism is an incomplete fusion of the spine during embryologic development and encompasses a spectrum ...
Lucy C, Holmes, Veetai, Li
openaire +2 more sources
Neurosurgery, 1978
Abstract Twelve patients with the clinical findings of spinal dysraphism form the basis for this report. In eight patients, physical findings, plain x-rays, and unenhanced spinal computed tomography allowed for precise diagnosis and subsequent therapy, without contrast myelography.
Hector E. James +2 more
openaire +3 more sources
Abstract Twelve patients with the clinical findings of spinal dysraphism form the basis for this report. In eight patients, physical findings, plain x-rays, and unenhanced spinal computed tomography allowed for precise diagnosis and subsequent therapy, without contrast myelography.
Hector E. James +2 more
openaire +3 more sources
Evaluation of Spinal Ultrasound in Spinal Dysraphism
Clinical Radiology, 2003The aims of this study were to evaluate the role of spinal ultrasound in detecting occult spinal dysraphism (OSD) in neonates and infants, and to determine the degree of agreement between ultrasound and magnetic resonance imaging (MRI) findings.Eighty-five consecutive infants had spinal ultrasound over 31 months.
Dominic Thompson
exaly +3 more sources
The Embryology of Spinal Dysraphism
Neurosurgery, 1983The theories of abnormal embryogenesis suggested as explanations for the various forms of SBA and occult spinal dysraphism appear in some instances too all encompassing, as in Gardner's hydrodynamic theory or Padget's neuroschisis theory, or too limited, as in the theory of arrested development proposed by Daniel and Strich for the ACM, or just too ...
openaire +2 more sources
The Journal of Bone and Joint Surgery. British volume, 1962
1. A syndrome resulting from congenital lesions affecting the spinal cord and cauda equina, associated with spina bifida occulta, is described. 2. The syndrome consists of a progressive deformity of the lower limbs in children. One foot and the same leg grow less rapidly than the other. The foot develops a progressive deformity which begins as a cavo-
C. C. Michael James, L. P. Lassman
openaire +1 more source
1. A syndrome resulting from congenital lesions affecting the spinal cord and cauda equina, associated with spina bifida occulta, is described. 2. The syndrome consists of a progressive deformity of the lower limbs in children. One foot and the same leg grow less rapidly than the other. The foot develops a progressive deformity which begins as a cavo-
C. C. Michael James, L. P. Lassman
openaire +1 more source
Archives of Neurology & Psychiatry, 1940
Since 1641, when Tulpuis 1 described a curious malformation of the spinal cord and the meninges to which he gave the name spina bifida, the medical literature has been replete with clinical, embryologic and pathologic reports of this condition. Despite the outstanding studies of von Recklinghausen 2 and the extensive works of Denuce, 3 Hesse, 4 ...
openaire +1 more source
Since 1641, when Tulpuis 1 described a curious malformation of the spinal cord and the meninges to which he gave the name spina bifida, the medical literature has been replete with clinical, embryologic and pathologic reports of this condition. Despite the outstanding studies of von Recklinghausen 2 and the extensive works of Denuce, 3 Hesse, 4 ...
openaire +1 more source
Spinal hamartoma associated with spinal dysraphism
Child's Nervous System, 2005The aims of the study were (1) to review the pathological findings of spinal lipomatous masses associated with congenital spinal dysraphism and (2) to discuss the pathological diagnosis.The pathological records of 47 patients at our institution were reviewed, and three illustrative cases were presented.Spinal tumorous lesions associated with spinal ...
Junji, Takeyama +6 more
openaire +2 more sources
Spinal dysraphism and the Currarino triad
Journal of Clinical Neuroscience, 1998A female born with a lumbosacral lipomyelomeningocele, an associated foot-shaped appendage attached to her sacrum, sacral dysgenesis, anal atresia, a recto-vaginal fistula and duplication of the right ureter is reported. We consider this case represents a pygomelus associated with a lipomyelomeningocele and an incomplete expression of Currarino's triad.
R J, Kahler, G S, Merry
openaire +2 more sources