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.
7. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome]. Witkowski R; Ullrich E; Pietsch P; Weber K; Heller K; Losanowa T; Nitz I Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109 [TBL] [Abstract][Full Text] [Related]
8. [Prader-Willi-Labhardt syndrome in a girl with development of an insulinoprivic diabete]. Battin J; Aubertin J; Alberty J; Fontan D Bord Med; 1970 Oct; 3(10):2462. PubMed ID: 5480225 [No Abstract] [Full Text] [Related]
10. [Congenital asymmetry and nervous system disorders in the Prader-Labhart-Willi syndrome]. Gaal K; Fazekas A; Vigvary L Kinderarztl Prax; 1972 Oct; 40(10):453-60. PubMed ID: 4650217 [No Abstract] [Full Text] [Related]
11. [Clinical data on the Prader-Labhart-Willi syndrome. I. New aspects of bone and eye involvement]. Fazekas A; Vígváry L; Nagy M; Bodnár L Orv Hetil; 1971 Jul; 112(29):1687-90. PubMed ID: 5111511 [No Abstract] [Full Text] [Related]
12. [Prader, Labhardt and Willi syndrome (study of 11 cases)]. Gabilan JC; Royer P Arch Fr Pediatr; 1968 Feb; 25(2):121-49. PubMed ID: 4386467 [No Abstract] [Full Text] [Related]
13. [De Sanctis-Cacchione syndrome (xeroderma pigmentosum with neurological complications)]. Yamamoto M; Fujino Z Nihon Ika Daigaku Zasshi; 1970 Jun; 37(3):259-63. PubMed ID: 5456594 [No Abstract] [Full Text] [Related]
14. [Report of case of Prader-Willi syndrome]. Visco G; Ughi M; Trevenzoli G Pediatr Med Chir; 1999; 21(3):149-50. PubMed ID: 10687166 [TBL] [Abstract][Full Text] [Related]
17. Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle East. Teebi AS; Al-Awadi SA; Farag TI; Naguib KK Am J Med Genet; 1986 Jun; 24(2):373-8. PubMed ID: 3717216 [No Abstract] [Full Text] [Related]
18. [Syndrome associated with adiposis, cryptorchism and mental retardation accompanied by a chromosomal aberration]. Roget J; Mouriquand C; Bernard Y; Patet J; Jobert J; Gilly C Pediatrie; 1965; 20(3):295-300. PubMed ID: 5827050 [No Abstract] [Full Text] [Related]
19. [Retinopapillary alterations during a neuro-endocrine syndrome of the Willi-Prader-Labardt type]. Bonn G; Dollfus MA; Polliot L; Richard M Bull Soc Ophtalmol Fr; 1971; 71(9):847-51. PubMed ID: 5151027 [No Abstract] [Full Text] [Related]