Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Majeed Al-Mateen"'
Publikováno v:
Developmental Medicine & Child Neurology. 35:631-636
Four infants developed dyskinesia after cardiopulmonary bypass surgery three to four days postoperatively. The dyskinesia was choreoathetotic, and involved mainly the mouth, tongue and face. It was absent during sleep. Three of these infants improved
Autor:
Majeed Al-Mateen, Lawrence Lavine, Sam J. Insalaco, Clayton A. Wiley, Ronald L. Hamilton, Kathryn McFadden, Guoji Wang
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 64:545-552
Neuronal intranuclear inclusion disease (NIID) is a rare and heterogeneous group of slowly progressive neurodegenerative disorders characterized by the widespread presence of eosinophilic neuronal intranuclear inclusions (NII) accompanied by a more r
Publikováno v:
Pediatric Neurology. 30:57-60
Wilson's disease is a genetic disorder of copper metabolism with a hepatic or neurologic presentation. A hepatic presentation is more common in young children. Neurologic Wilson's disease often manifests as a movement disorder with dystonia, tremor,
Autor:
Margaret Hood, Kari J. Vitikainen, Don Trippel, Majeed Al-Mateen, Randolph K. Otto, Samuel J. Insalaco
Publikováno v:
Pediatrics. 112:e162-e167
We describe 2 children with cerebrovascular events caused by emboli from left atrial myxomas and review 7 other pediatric cases from the literature. Transient cutaneous eruptions involving the extremities preceded the cerebrovascular events and were
Publikováno v:
Pediatrics. 107:930-934
Publikováno v:
Journal of child neurology. 29(3)
We describe 2 patients with X-linked Charcot-Marie-Tooth disease, type 1 (CMTX1) disease and central nervous system manifestations and review 19 cases from the literature. Our first case had not been previously diagnosed with Charcot-Marie-Tooth dise
Autor:
Shen, Xin‐Ming1 (AUTHOR) shen.xinming@mayo.edu, Nakata, Tomohiko2,3 (AUTHOR), Mizuno, Seiji4 (AUTHOR), Imoto, Issei5 (AUTHOR), Selcen, Duygu1 (AUTHOR), Ohno, Kinji2 (AUTHOR) ohnok@med.nagoya-u.ac.jp, Engel, Andrew G.1 (AUTHOR)
Publikováno v:
Annals of Clinical & Translational Neurology. May2023, Vol. 10 Issue 5, p732-743. 12p.
Publikováno v:
American Journal of Diseases of Children. 140:761
• We report 15 cases of Rett syndrome, a slowly progressive disorder that occurs only in girls and is characterized by early deterioration of higher brain function with dementia and autistic behavior, loss of purposeful use of the hands, and decele
Publikováno v:
Journal of Child Neurology; Mar2014, Vol. 29 Issue 3, p342-348, 7p
Publikováno v:
American Journal of Psychiatry; Aug2006, Vol. 163 Issue 8, p1464-1477, 14p