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.
67 related articles for article (PubMed ID: 1801825)
1. A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features. Richardson RJ; Kirk J Arch Dis Child; 1991 Nov; 66(11):1365. PubMed ID: 1801825 [No Abstract] [Full Text] [Related]
2. A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features. Sanjad SA; Sakati NA; Abu-Osba YK; Kaddoura R; Milner RD Arch Dis Child; 1991 Feb; 66(2):193-6. PubMed ID: 2001103 [TBL] [Abstract][Full Text] [Related]
3. The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patients. Hershkovitz E; Shalitin S; Levy J; Leiberman E; Weinshtock A; Varsano I; Gorodischer R Isr J Med Sci; 1995 May; 31(5):293-7. PubMed ID: 7538982 [TBL] [Abstract][Full Text] [Related]
4. Congenital hypoparathyroidism, seizure, extreme growth failure with developmental delay and dysmorphic features--another case of this new syndrome. Kalam MA; Hafeez W Clin Genet; 1992 Sep; 42(3):110-3. PubMed ID: 1395080 [TBL] [Abstract][Full Text] [Related]
5. Congenital hypoparathyroidism. Laron Z Isr J Med Sci; 1995 May; 31(5):326-7. PubMed ID: 7759229 [No Abstract] [Full Text] [Related]
6. The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies. al-Gazali LI; Dawodu A Clin Dysmorphol; 1997 Jul; 6(3):233-7. PubMed ID: 9220193 [TBL] [Abstract][Full Text] [Related]
7. Short stature, mental retardation, and hypoparathyroidism: a new syndrome. Richardson RJ; Kirk JM Arch Dis Child; 1990 Oct; 65(10):1113-7. PubMed ID: 1701077 [TBL] [Abstract][Full Text] [Related]
9. Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43. Kelly TE; Blanton S; Saif R; Sanjad SA; Sakati NA J Med Genet; 2000 Jan; 37(1):63-4. PubMed ID: 10691411 [No Abstract] [Full Text] [Related]
10. Congenital primary hypoparathyroidism presented with extensive cutaneous and subcutaneous calcifications. Aslan Y; Gedik Y; Okten A; Aksoy A; Cimşit G; Ari N Turk J Pediatr; 1999; 41(2):253-7. PubMed ID: 10770667 [TBL] [Abstract][Full Text] [Related]
11. Hypoparathyroidism, retardation, and dysmorphism syndrome: impaired early growth and increased susceptibility to severe infections due to hyposplenism and impaired polymorphonuclear cell functions. Hershkovitz E; Rozin I; Limony Y; Golan H; Hadad N; Gorodischer R; Levy R Pediatr Res; 2007 Oct; 62(4):505-9. PubMed ID: 17667846 [TBL] [Abstract][Full Text] [Related]
12. Facio-auriculo-vertebral sequence in association with congenital hypoparathyroidism. Patil MB; Patil SM Indian Pediatr; 2012 Aug; 49(8):670-2. PubMed ID: 22962243 [TBL] [Abstract][Full Text] [Related]
13. Congenital familial hypoparathyroidism. Management of an infant, genetics, pathogenesis of hypoparathyroidism, and fetal undermineralization. Gorodischer R; Aceto T; Terplan K Am J Dis Child; 1970 Jan; 119(1):74-8. PubMed ID: 5308088 [No Abstract] [Full Text] [Related]
17. Surgical closure of an atrial septal defect in an 11-year-old girl with Silver-Russell syndrome. Vahlas CE; Chatzis AC; Giannopoulos NM; Contrafouris CA; Milonakis MC; Sarris GE J Cardiovasc Med (Hagerstown); 2007 Oct; 8(10):850-1. PubMed ID: 17885526 [TBL] [Abstract][Full Text] [Related]
18. A patient with hypoparathyroidism, dysmorphic features and mental retardation. Cohen SE; Raz I; Safadi R Eur J Med Res; 1996 Feb; 1(5):266-8. PubMed ID: 9374448 [TBL] [Abstract][Full Text] [Related]
19. New findings in a patient with Dubowitz syndrome: velopharyngeal insufficiency and hypoparathyroidism. Lerman-Sagie T; Merlob P; Shuper A; Kauli R; Kozokaro Z; Grunebaum M; Mimouni M Am J Med Genet; 1990 Oct; 37(2):241-3. PubMed ID: 2248292 [TBL] [Abstract][Full Text] [Related]
20. Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion. Akçakuş M; Güneş T; Kurtoğlu S; Cetin N; Ozkul Y; Narin N; Atabek ME; Uğraş R Turk J Pediatr; 2004; 46(2):191-3. PubMed ID: 15214756 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]