S Dreborg, A Erikson, B Hagberg - European Journal of Pediatrics, 1980 - Springer Abstract. We report follow-up studies of 22 cases of the Norrbottnian type of Gaucher disease
("type III"). The series was divided into 2 main groups of families depending on their birth province
(Norrbotten, VS.ster- botten). The distribution and types of organ mani- festations and ... Cited by 68 - Related articles - All 2 versions
- ►oxfordjournals.org [PDF] O Neudorfer, N Giladi, D Elstein, A Abrahamov, T … - Qjm, 1996 - Oxford Univ Press From the Gaucher Clinic, Department of Medicine, Shaare-Zedek Medical Center,
Jerusalem, Israel, 1 Department of Neurology and 2 Institute of Hematology, Carmel
Hospital, Haifa, Israel, 3 Department of Neurology, Hadassah University Hospital, ... Cited by 64 - Related articles - BL Direct - All 3 versions
- ►caltech.edu [PDF] K Wong, E Sidransky, A Verma, T Mixon, GD … - Molecular genetics and …, 2004 - Elsevier To better understand the pathogenesis of brain dysfunction in Gaucher disease (GD), we studied
brain pathology in seven subjects with type 1 GD (four also exhibited parkinsonism and
dementia), three with type 2 GD and four with type 3 GD. Unique pathologic patterns of ... Cited by 63 - Related articles - All 6 versions
EL Schneider, CJ Epstein, MJ Kaback, D Brandes - The American journal of …, 1977 - Elsevier Three patients with “adult” Gaucher's disease with severe pulmonary involvement are
described. The clinical course of these patients was characterized by hepatosplenomegaly in
infancy, followed by the juvenile onset of dyspnea culminating in pulmonary failure and ... Cited by 51 - Related articles - All 3 versions
DG Cogan, FC Chu, D Reingold, J … - Archives of …, 1981 - archopht.highwire.org • Ocular motor disturbances are de¬ scribed with a miscellany of metabolic disturbances. Horizontal
gaze abnormali¬ ties, often simulating congenital ocular motor apraxia, characterized Gaucher's
disease. Vertical gaze abnormalities, es¬ pecially downgaze paralysis, character¬ ized ... Cited by 45 - Related articles - All 3 versions
E Uyama, K Takahashi, M Owada, R … - Acta Neurologica …, 1992 - interscience.wiley.com We describe three adult siblings with communicating hydrocephalus, corneal opacities,
deafness, valvular heart disease, and deformed toes associated with glucosylceramide
(glc-cer)-β-glucosidase deficiency. The common manifestations of Gaucher disease were ... Cited by 43 - Related articles - BL Direct - All 3 versions
[CITATION] Supranuclear disorders of eye movements
RB DAROFF, BT TROOST - Neuro-ophthalmology: Joel S. …, 1978 - HarperCollins Publishers Cited by 39 - Related articles
LN Clark, A Nicolai, S Afridi, J Harris, H Mejia … - Movement …, 2005 - interscience.wiley.com It is also possible that your web browser is not configured or not able to display style sheets.
In this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the latest version of Microsoft or Mozilla web browser to ... Cited by 35 - Related articles - All 3 versions
- ►bmj.com [PDF] JO King - Journal of Neurology, Neurosurgery, and Psychiatry, 1975 - pubmedcentral.nih.gov By progressive myoclonic epilepsyis meant the striking combination of grand mal seizures and
generalized myoclonus which, in some instances, may be associated with intellectual
deterioration. A mild degree ofmyoclonic jerking is common in epileptics, particularly ... Cited by 32 - Related articles - All 5 versions
JF Neil, RH Glew, SP Peters - Archives of Neurology, 1979 - archneur.highwire.org \s=b\A family is described in which adult-$ onset Gaucher's disease developed, fol- lowed years
later by atypical psychotic disorders with neurologic and electroen- cephalographic
abnormalities. A bio- chemical investigation of primary and secondary enzyme alterations ... Cited by 24 - Related articles - All 3 versions
