171 related articles for article (PubMed ID: 9018418)
1. Identical twins with the classical form of Schwartz-Jampel syndrome.
Pinto-Escalante D; Ceballos-Quintal JM; Canto-Herrera J
Clin Dysmorphol; 1997 Jan; 6(1):45-9. PubMed ID: 9018418
[TBL] [Abstract][Full Text] [Related]
2. Schwartz-Jampel syndrome: an atypical form?
Figuera LE; Jimenez-Gil FJ; García-Cruz MO; Cantú JM
Am J Med Genet; 1993 Sep; 47(4):526-8. PubMed ID: 8256816
[TBL] [Abstract][Full Text] [Related]
3. The Schwartz-Jampel syndrome.
al Gazali LI
Clin Dysmorphol; 1993 Jan; 2(1):47-54. PubMed ID: 8298738
[TBL] [Abstract][Full Text] [Related]
4. Schwartz Jampel syndrome in children.
Arya R; Sharma S; Gupta N; Kumar S; Kabra M; Gulati S
J Clin Neurosci; 2013 Feb; 20(2):313-7. PubMed ID: 23219824
[TBL] [Abstract][Full Text] [Related]
5. [Cloverleaf skull associated with generalized bone defects close to asphyxiating thoracic dysplasia].
Benallègue A; Lacete F; Maroteaux P
Ann Genet; 1987; 30(2):113-7. PubMed ID: 3499843
[TBL] [Abstract][Full Text] [Related]
6. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome.
Nevin NC; Thomas PS; Hutchinson J
Am J Med Genet; 1986 May; 24(1):33-9. PubMed ID: 3706411
[TBL] [Abstract][Full Text] [Related]
7. Schwartz Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation.
Gürbüz G; Albayrak HM
Turk J Pediatr; 2019; 61(6):967-970. PubMed ID: 32134596
[TBL] [Abstract][Full Text] [Related]
8. Neonatal manifestations of Schwartz-Jampel syndrome.
Farrell SA; Davidson RG; Thorp P
Am J Med Genet; 1987 Aug; 27(4):799-805. PubMed ID: 3321990
[TBL] [Abstract][Full Text] [Related]
9. [Schwartz-Jampel syndrome (osteochondromuscular dystrophy)].
Ben Becher S; el Mabrouk J; Debbiche A; Hammou A; Ghram N; Makni S; Boudhina T
Arch Fr Pediatr; 1992 Nov; 49(9):799-802. PubMed ID: 1300968
[TBL] [Abstract][Full Text] [Related]
10. Schwartz-Jampel syndrome: a review of the literature and case report.
Mallineni SK; Yiu CK; King NM
Spec Care Dentist; 2012 Jun; 32(3):105-11. PubMed ID: 22591433
[TBL] [Abstract][Full Text] [Related]
11. Schwartz-Jampel syndrome: three pediatric case reports.
Yapicioğlu H; Satar M; Yildizdaş D; Narli N; Suleymanova D; Tutak E
Genet Couns; 2003; 14(3):353-8. PubMed ID: 14577682
[TBL] [Abstract][Full Text] [Related]
12. Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.
Brown KA; al-Gazali LI; Moynihan LM; Lench NJ; Markham AF; Mueller RF
J Med Genet; 1997 Aug; 34(8):685-7. PubMed ID: 9279765
[TBL] [Abstract][Full Text] [Related]
13. [Clinical analysis of four patients with Schwartz-Jampel syndrome].
Zhang S; Wu HS; Lü JL
Zhonghua Er Ke Za Zhi; 2012 Mar; 50(3):231-4. PubMed ID: 22801212
[TBL] [Abstract][Full Text] [Related]
14. Botulinum toxin A injections for the treatment of Schwartz-Jampel syndrome: a case series.
Aburahma SK; Al-Khateeb T; Alrefai A; Amarin Z
J Child Neurol; 2009 Jan; 24(1):5-8. PubMed ID: 19168812
[TBL] [Abstract][Full Text] [Related]
15. A case of Schwartz-Jampel syndrome with cleft palate.
Abdel-Aziz M; Azab NA
Int J Pediatr Otorhinolaryngol; 2009 Nov; 73(11):1601-3. PubMed ID: 19733405
[TBL] [Abstract][Full Text] [Related]
16. Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2.
Cormier-Daire V; Superti-Furga A; Munnich A; Lyonnet S; Rustin P; Delezoide AL; De Lonlay P; Giedion A; Maroteaux P; Le Merrer M
Am J Med Genet; 1998 Jun; 78(2):146-9. PubMed ID: 9674905
[TBL] [Abstract][Full Text] [Related]
17. Schwartz-Jampel syndrome with gastroduodenal bleeding.
Polat İ; Karaoğlu P; Yiş U; Kurul SH
J Pediatr Neurosci; 2016; 11(3):255-257. PubMed ID: 27857801
[TBL] [Abstract][Full Text] [Related]
18. [Clinical and genetic features of Schwartz-Jampel syndrome in a Chinese child: case report and literature review].
Dai L; Fang F; Huang Y; Cheng H; Ren C
Zhonghua Er Ke Za Zhi; 2015 Nov; 53(11):855-9. PubMed ID: 26758326
[TBL] [Abstract][Full Text] [Related]
19. Trichorhinophalangeal syndrome type I in monozygotic twins discordant for hip pathology. Report on the morphological evolution of cone-shaped epiphyses and the unusual pattern of skeletal maturation.
Naselli A; Vignolo M; Di Battista E; Papale V; Aicardi G; Becchetti S; Tomà P
Pediatr Radiol; 1998 Nov; 28(11):851-5. PubMed ID: 9799317
[TBL] [Abstract][Full Text] [Related]
20. Schwartz-Jampel syndrome: report of one case.
Yang MT; Yang CC; Chu LW; Lee WT; Young C; Wang PJ
Acta Paediatr Taiwan; 2002; 43(4):220-3. PubMed ID: 12238912
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]