94 related articles for article (PubMed ID: 569297)
1. Growth deficiency dysmorphic syndromes.
Smith DW
Postgrad Med J; 1978; 54 Suppl 1():147-57. PubMed ID: 569297
[TBL] [Abstract][Full Text] [Related]
2. Is complete catch-up possible for stunted malnourished children?
Golden MH
Eur J Clin Nutr; 1994 Feb; 48 Suppl 1():S58-70; discussion S71. PubMed ID: 8005092
[TBL] [Abstract][Full Text] [Related]
3. [Silver-Russel Syndrome in aa 13-month old girl].
Hajdas-Kudela I; Jamroz E; Marszał E
Pol Merkur Lekarski; 1997 Jun; 2(12):387-8. PubMed ID: 9424332
[TBL] [Abstract][Full Text] [Related]
4. Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.
Niikawa N; Kuroki Y; Kajii T; Matsuura N; Ishikiriyama S; Tonoki H; Ishikawa N; Yamada Y; Fujita M; Umemoto H
Am J Med Genet; 1988 Nov; 31(3):565-89. PubMed ID: 3067577
[TBL] [Abstract][Full Text] [Related]
5. Introduction to the study of pre- and postnatal growth in humans: a review.
Mendez H
Am J Med Genet; 1985 Jan; 20(1):63-85. PubMed ID: 3881956
[TBL] [Abstract][Full Text] [Related]
6. [Natural history of intrauterine growth retardation: pubertal growth and adult height].
Job JC; Rolland A
Arch Fr Pediatr; 1986 May; 43(5):301-6. PubMed ID: 3778088
[TBL] [Abstract][Full Text] [Related]
7. Ocular abnormalities in the fetal alcohol syndrome.
Strömland K
Acta Ophthalmol Suppl (1985); 1985; 171():1-50. PubMed ID: 2988263
[TBL] [Abstract][Full Text] [Related]
8. Growth characteristics of children with ectodermal dysplasia syndromes.
Motil KJ; Fete TJ; Fraley JK; Schultz RJ; Foy TM; Ochs U; Sybert VP
Pediatrics; 2005 Aug; 116(2):e229-34. PubMed ID: 16061575
[TBL] [Abstract][Full Text] [Related]
9. Onset and evolution of stunting in infants and children. Examples from the Human Nutrition Collaborative Research Support Program. Kenya and Egypt studies.
Neumann CG; Harrison GG
Eur J Clin Nutr; 1994 Feb; 48 Suppl 1():S90-102. PubMed ID: 8005095
[TBL] [Abstract][Full Text] [Related]
10. Recognizable patterns of human malformation.
Smith DW
Major Probl Clin Pediatr; 1976; 7():1-497. PubMed ID: 940360
[No Abstract] [Full Text] [Related]
11. [A cytogenetic study of the functions of the variable regions in human C heterochromatin. I. The effect of C heterochromatin on gene expression].
Podugol'nikov OA; Solonichenko VG
Tsitologiia; 1994; 36(11):1035-40. PubMed ID: 7709464
[TBL] [Abstract][Full Text] [Related]
12. [Growth in height, bone and endocrine abnormalities in hypoplasia of the intrahepatic bile ducts. Eleven cases].
Courtecuisse V; Dommergues JP; Girard F; Limal JM
Ann Pediatr (Paris); 1976 Sep; 23(8-9):525-31. PubMed ID: 16104187
[No Abstract] [Full Text] [Related]
13. Presence of magnetic resonance imaging abnormalities of the hypothalamic-pituitary axis is a significant determinant of the first 3 years growth response to human growth hormone treatment in prepubertal children with nonacquired growth hormone deficiency.
Zenaty D; Garel C; Limoni C; Czernichow P; Léger J
Clin Endocrinol (Oxf); 2003 May; 58(5):647-52. PubMed ID: 12699449
[TBL] [Abstract][Full Text] [Related]
14. [The fetal alcohol syndrome. Description of 2 cases].
Baldassar Ferrero AM; De Sario R; Miglio C; Stradoni P
Ann Osp Maria Vittoria Torino; 1982; 25(7-12):215-25. PubMed ID: 7187854
[TBL] [Abstract][Full Text] [Related]
15. Role of magnetic resonance imaging in the diagnosis and prognosis of growth hormone deficiency.
Bozzola M; Adamsbaum C; Biscaldi I; Zecca M; Cisternino M; Genovese E; Richard I; Kalifa G; Chaussain JL
Clin Endocrinol (Oxf); 1996 Jul; 45(1):21-6. PubMed ID: 8796134
[TBL] [Abstract][Full Text] [Related]
16. Birth outcomes of cases with unclassified multiple congenital abnormalities and pregnancy complications in their mothers depending on the number of component defects. Population-based case-control study.
Puhó EH; Czeizel AE; Acs N; Bánhidy F
Congenit Anom (Kyoto); 2008 Sep; 48(3):126-36. PubMed ID: 18778457
[TBL] [Abstract][Full Text] [Related]
17. [Congenital skeletal malformations and their treatment].
Sulamaa M; Ryöppy S
Duodecim; 1968; 84(18):1051-67. PubMed ID: 5706121
[No Abstract] [Full Text] [Related]
18. [Prenatal diagnosis of skeletal dysplasia: case report of a fetus with multiple anomalies].
Novakov Mikić A; Stojić S; Konstantinidis G; Ristivojević A; Krnojelac D
Med Pregl; 2000; 53(3-4):197-201. PubMed ID: 10965689
[TBL] [Abstract][Full Text] [Related]
19. Age and height at diagnosis in Turner syndrome: influence of parental height.
Massa GG; Vanderschueren-Lodeweyckx M
Pediatrics; 1991 Dec; 88(6):1148-52. PubMed ID: 1956730
[TBL] [Abstract][Full Text] [Related]
20. Antenatal manifestations of mitochondrial respiratory chain deficiency.
von Kleist-Retzow JC; Cormier-Daire V; Viot G; Goldenberg A; Mardach B; Amiel J; Saada P; Dumez Y; Brunelle F; Saudubray JM; Chrétien D; Rötig A; Rustin P; Munnich A; De Lonlay P
J Pediatr; 2003 Aug; 143(2):208-12. PubMed ID: 12970634
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]