Results 251 to 260 of about 108,027 (308)

Neurofibroma of cranial nerve X in von Recklinghausen disease

, 2011
openaire   +1 more source

Neurotrophic keratopathy in childhood: advances in understanding of pathogenesis and management. [PDF]

Eye (Lond)
Jiang J, Ashton CBJ, Larkin DFP.
europepmc   +1 more source

Cadaveric addendum to the consensus on ultrasound‐based lymph‐node staging in gynecological cancer

Ultrasound in Obstetrics &Gynecology, EarlyView.
D. Fischerova, E. Farsi, E. Facchetti, E. Panizzolo, G. Gambino, H. Reina, F. Sousa, M. R. Kadajari, N. Tiszlavicz, G. Garganese, O. Nanka, Collaborators, E. Gatti, C. Culcasi   +13 more
wiley   +1 more source

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Cerebrovascular Brainstem Diseases with Isolated Cranial Nerve Palsies

Cerebrovascular Diseases, 2002
There is a significant number of individual patients with cranial nerve palsies as the sole manifestation of MRI- and, less frequently, CT-documented small brainstem infarctions or hemorrhages. The 3rd and 6th nerves are most commonly involved and, less frequently, the 4th, 5th, 7th, and 8th nerves.
Frank, Thömke, Ludwig, Gutmann, Peter, Stoeter, Hanns Christian, Hopf   +3 more
openaire   +2 more sources

Cranial nerve involvement in Charcot–Marie–Tooth Disease

Journal of Clinical Neuroscience, 2017
Charcot-Marie-Tooth Disease (CMT) is a rare disorder with less than 200,000 cases reported in the US every year, making diagnosis challenging. MR and CT imaging has become more common in the evaluation of CMT to identify areas of disease involvement.A 27-year-old female from Guatemala with a past history of polio initially presented to the emergency ...
Nirav Das, Savannah Kandalaft, Xiao Wu, Ajay Malhotra   +3 more
openaire   +2 more sources

Multiple cranial nerve enlargement in Charcot-Marie-Tooth disease

Journal of Neurology, Neurosurgery & Psychiatry, 2020
Hypertrophy of peripheral nerves are commonly reported in patients with demyelinating forms of Charcot-Marie-Tooth disease (CMT).1 Herein, an under-recognised association with hypertrophy of multiple cranial nerves in a patient with CMT is described. A 39-year-old otherwise healthy man presented with a 2-month history of tension-type headaches without
William Huynh, Lynette Masters
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Multiple cranial nerve enhancement in early infantile Krabbe’s disease

Neurology, 2000
Krabbe’s disease or globoid-cell leukodystrophy is an autosomal recessive disorder caused by a mutation of the galactocerebroside beta-galactosidase gene located at chromosome 14q31.1 The reduction of enzymatic activity affects the catabolism of galactosylceramide to ceramide and galactose.1 This disorder is characterized by an abnormal breakdown and ...
O G, Bernal, N, Lenn
openaire   +2 more sources