189 related articles for article (PubMed ID: 6068089)
1. Prader--Willi syndrome.
Hoefnagel D; Costello PJ; Hatoum K
J Ment Defic Res; 1967 Mar; 11(1):1-11. PubMed ID: 6068089
[No Abstract] [Full Text] [Related]
2. Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation).
Jancar J
J Ment Defic Res; 1971 Mar; 15(1):20-9. PubMed ID: 5581387
[No Abstract] [Full Text] [Related]
3. [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]
4. Prader-Willi syndrome.
Juul J; Dupont A
J Ment Defic Res; 1967 Mar; 11(1):12-22. PubMed ID: 6034523
[No Abstract] [Full Text] [Related]
5. [The Prader-Willi syndrome].
Lydecken K
Duodecim; 1967; 83(22):1285-8. PubMed ID: 5594519
[No Abstract] [Full Text] [Related]
6. [Prader-Labhart-Willi syndrome diagnosed in a newborn].
Ferenczy I; Péter J; Rixer G; Schaff Z
Orv Hetil; 1971 Jan; 112(3):137-40. PubMed ID: 5540532
[No Abstract] [Full Text] [Related]
7. [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]
8. [Prader-Labhardt-Willi syndrome].
Bayart-Gennequin F; Poissonnier D; Farriaux JP; Fontaine G
Lille Med; 1970; 15(6):982-8. PubMed ID: 5454736
[No Abstract] [Full Text] [Related]
9. [H20 (hypotonia, hypomentia and obesity) syndrome].
Ueda K; Sugawara S
Nihon Rinsho; 1969 May; 27(5):1510-1. PubMed ID: 5817515
[No Abstract] [Full Text] [Related]
10. [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]
11. Hereditary deafness in man.
Konigsmark BW
N Engl J Med; 1969 Oct; 281(14):774-8 contd. PubMed ID: 4185450
[No Abstract] [Full Text] [Related]
12. X-linked syndrome of congenital ichthyosis, hypogonadism, mental retardation and anosmia.
Perrin JC; Idemoto JY; Sotos JF; Maurer WF; Steinberg AG
Birth Defects Orig Artic Ser; 1976; 12(5):267-74. PubMed ID: 182300
[No Abstract] [Full Text] [Related]
13. Hypogonadism in Prader-Willi syndrome.
Wannarachue N; Ruvalcaba RH
Am J Ment Defic; 1975 Mar; 79(5):592-603. PubMed ID: 164772
[TBL] [Abstract][Full Text] [Related]
14. [Endocrine interrelations in diabetes mellitus in children].
Barta L
Arch Kinderheilkd; 1969 May; 179(1):7-16. PubMed ID: 4240561
[No Abstract] [Full Text] [Related]
15. Forme fruste of the Prader-Willi syndrome (HHHO) and balanced D-E translocation.
Schneider HJ; Zellweger H
Helv Paediatr Acta; 1968 Apr; 23(2):128-35. PubMed ID: 4387003
[No Abstract] [Full Text] [Related]
16. [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]
17. [Prader-Labhart-Willi syndrome. II. Neurologic implications].
Gaál K
Orv Hetil; 1971 Aug; 112(33):1968-70. PubMed ID: 5166622
[No Abstract] [Full Text] [Related]
18. [Prader-Labhart-Wille-Fanconi syndrome].
Schmuck L; Auerswald W; Oehlke W
Z Gesamte Inn Med; 1972 Jul; 27(14):627-30. PubMed ID: 5082878
[No Abstract] [Full Text] [Related]
19. [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]
20. 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]
[Next] [New Search]
