148 related articles for article (PubMed ID: 10832484)
1. Hypomelanosis of Ito.
Kumar A; Chaudhary D; Bhargava V
Indian J Pediatr; 1996; 63(4):573-5. PubMed ID: 10832484
[TBL] [Abstract][Full Text] [Related]
2. Hypomelanosis of Ito. Report of a case and review of the literature.
Buzas JW; Sina B; Burnett JW
J Am Acad Dermatol; 1981 Feb; 4(2):195-204. PubMed ID: 7217390
[TBL] [Abstract][Full Text] [Related]
3. Hypomelanosis of Ito.
Kulkarni ML; Kumar CS; Venkataramana V; Reddy EV
Indian Pediatr; 1996 Mar; 33(3):243-5. PubMed ID: 8772851
[No Abstract] [Full Text] [Related]
4. [Hypomelanosis Ito in translocation trisomy 9/mosaicism (46,XX/46,XX,t(9;9)(p24;p24)). Spontaneous remission in childhood].
Dereser-Dennl M; Brude E; König R
Hautarzt; 2000 Sep; 51(9):688-92. PubMed ID: 11057398
[TBL] [Abstract][Full Text] [Related]
5. Ring chromosome 17 in a mentally retarded boy.
Qazi OH; Madahar C; Kanchanapoomi R; Giridharan R; Beller E
Ann Genet; 1979; 22(4):234-8. PubMed ID: 121681
[TBL] [Abstract][Full Text] [Related]
6. Hypomelanosis of Ito (incontinentia pigmenti achromians).
Gordon N
Dev Med Child Neurol; 1994 Mar; 36(3):271-4. PubMed ID: 7511121
[No Abstract] [Full Text] [Related]
7. Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasia.
Wulfsberg EA; Wassel WC; Polo CA
Clin Genet; 1991 May; 39(5):370-5. PubMed ID: 1860253
[TBL] [Abstract][Full Text] [Related]
8. Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.
Pavone V; Signorelli SS; Praticò AD; Corsello G; Savasta S; Falsaperla R; Pavone P; Sessa G; Ruggieri M
Medicine (Baltimore); 2016 Mar; 95(10):e2705. PubMed ID: 26962770
[TBL] [Abstract][Full Text] [Related]
9. Studies on chromosomal anomaly syndrome with epilepsy.
Sugama S; Akatsuka A; Ochiai Y; Tsuzura S; Maekawa K
Jpn J Psychiatry Neurol; 1993 Jun; 47(2):283-5. PubMed ID: 8271565
[No Abstract] [Full Text] [Related]
10. Familial hypomelanosis of Ito.
Montagna P; Procaccianti G; Galli G; Ripamonti L; Patrizi A; Baruzzi A
Eur Neurol; 1991; 31(6):345-7. PubMed ID: 1756756
[TBL] [Abstract][Full Text] [Related]
11. Hypomelanosis of Ito in three cases with autism and autistic-like conditions.
Akefeldt A; Gillberg C
Dev Med Child Neurol; 1991 Aug; 33(8):737-43. PubMed ID: 1717328
[TBL] [Abstract][Full Text] [Related]
12. Hypomelanosis of Ito: diagnostic criteria and report of 41 cases.
Ruiz-Maldonado R; Toussaint S; Tamayo L; Laterza A; del Castillo V
Pediatr Dermatol; 1992 Mar; 9(1):1-10. PubMed ID: 1574469
[TBL] [Abstract][Full Text] [Related]
13. Hypomelanosis of ito.
Singh SA; Sampath S; Nathan R; Nair M
Indian J Pediatr; 2004 Oct; 71(10):947. PubMed ID: 15531845
[TBL] [Abstract][Full Text] [Related]
14. Ring chromosome 14: a distinct clinical entity.
Schmidt R; Eviatar L; Nitowsky HM; Wong M; Miranda S
J Med Genet; 1981 Aug; 18(4):304-7. PubMed ID: 7277427
[TBL] [Abstract][Full Text] [Related]
15. [Hypomelanosis of Ito: autism, segmental dilatation of colon and unusual neuroimaging findings].
Hermida A; Eirís J; Alvarez-Moreno A; Alonso-Martín A; Barreiro J; Castro-Gago M
Rev Neurol; 1997 Jan; 25(137):71-4. PubMed ID: 9091225
[TBL] [Abstract][Full Text] [Related]
16. A ring-20 chromosome.
Atkins L; Miller WL; Salam M
J Med Genet; 1972 Sep; 9(3):377-80. PubMed ID: 4627939
[No Abstract] [Full Text] [Related]
17. Glomerulocystic kidney disease in hypomelanosis of Ito.
Vergine G; Mencarelli F; Diomedi-Camassei F; Caridi G; El Hachem M; Ghiggeri GM; Emma F
Pediatr Nephrol; 2008 Jul; 23(7):1183-7. PubMed ID: 18392644
[TBL] [Abstract][Full Text] [Related]
18. Hypomelanosis of Ito with triphalangeal thumbs.
Kukolich MK; Althaus BW; Freeman MV; Lewandowski RC
J Med Genet; 1980 Apr; 17(2):151-2. PubMed ID: 7381873
[TBL] [Abstract][Full Text] [Related]
19. Ito syndrome (hypomelanosis of Ito) as a cause of intractable epilepsy.
Hara M; Mitsuishi Y; Yajima K; Kozasa M; Saito K; Fukuyama Y
Jpn J Psychiatry Neurol; 1989 Sep; 43(3):487-9. PubMed ID: 2516560
[No Abstract] [Full Text] [Related]
20. Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hair.
Ozand PT; Waghray M; Cook JD; Sheth K; Gascon GG
J Child Neurol; 1992 Apr; 7 Suppl():S79-82. PubMed ID: 1588019
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]