These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
143 related articles for article (PubMed ID: 5824822)
21. [Sjögren-Larsson syndrome (contribution of 2 cases with familial features]. Anibaldi A; Cieri E; Finocchi G Minerva Pediatr; 1967 Mar; 19(11):483-7. PubMed ID: 5611127 [No Abstract] [Full Text] [Related]
22. [A clinical study of cerebral palsy in Shiga; 1977-1986--II. Severity of the disability and complications in various types of cerebral palsy]. Suzuki J; Ito M; Tomiwa K; Okuno T No To Hattatsu; 1999 Jul; 31(4):336-42. PubMed ID: 10429483 [TBL] [Abstract][Full Text] [Related]
23. A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency. Jameel M; Klar J; Tariq M; Moawia A; Altaf Malik N; Seema Waseem S; Abdullah U; Naeem Khan T; Raininko R; Baig SM; Dahl N BMC Med Genet; 2014 Dec; 15():133. PubMed ID: 25496299 [TBL] [Abstract][Full Text] [Related]
24. A Bucharest-district prevalence survey of low-grade mental deficiency among 7- to 15-year-old children. Christodorescu D; Retezeanu A; Bălăiţă C; Berbescu A ; Sîrbu C; Ciupitu A Neurol Psychiatr (Bucur); 1976; 14(4):311-8. PubMed ID: 139674 [No Abstract] [Full Text] [Related]
25. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome. Clayton-Smith J; Webb T; Cheng XJ; Pembrey ME; Malcolm S J Med Genet; 1993 Jun; 30(6):529-31. PubMed ID: 8326502 [TBL] [Abstract][Full Text] [Related]
26. POSTURAL REACTIONS IN 100 CHILDREN WITH CEREBRAL PALSY AND MENTAL HANDICAP. ZAPPELLA M Dev Med Child Neurol; 1964 Oct; 6():475-84. PubMed ID: 14215225 [No Abstract] [Full Text] [Related]
35. Familial 13p+ chromosome with mental retardation and dysmorphic features of two children. Stoll C; Rohmer A; Korn R; Heumann G Hum Genet; 1976 Sep; 34(1):81-4. PubMed ID: 965011 [TBL] [Abstract][Full Text] [Related]
36. Familial microcephaly with severe neurological deficits: a description of five affected siblings. Gross-Tsur V; Joseph A; Blinder G; Amir N Clin Genet; 1995 Jan; 47(1):33-7. PubMed ID: 7774041 [TBL] [Abstract][Full Text] [Related]
37. A survey of cerebral palsy in Windsor and Essex County, Ontario. McGreal DA Can Med Assoc J; 1966 Dec; 95(24):1237-40. PubMed ID: 5954487 [No Abstract] [Full Text] [Related]
38. Familial ataxic diplegia with deficient cellular immunity. A new clinical entity. Hagberg B; Hansson O; Lidén S; Nilsson K Acta Paediatr Scand; 1970 Sep; 59(5):545-50. PubMed ID: 5455521 [No Abstract] [Full Text] [Related]
39. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus. Rosenthal IM; Krmpotic E; Bocian M; Szego K Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842 [No Abstract] [Full Text] [Related]