162 related articles for article (PubMed ID: 35109856)
1. Congenital anomalies-associated Riga-Fede disease as an early manifestation of Lesch-Nyhan syndrome: rare entities in the same pediatric patient-a case report.
Eita AAB
BMC Oral Health; 2022 Feb; 22(1):26. PubMed ID: 35109856
[TBL] [Abstract][Full Text] [Related]
2. Cerebral Venous Sinus Thrombosis in a Child with Lesch-Nyhan Syndrome.
Manokaran RK; Jauhari P; Chakrabarty B; Gupta N; Kumar A; Gulati S
Neurol India; 2021; 69(4):1021-1023. PubMed ID: 34507434
[TBL] [Abstract][Full Text] [Related]
3. Rare variant of Lesch-Nyhan syndrome without self-mutilation or nephrolithiasis.
Kersnik Levart T
Pediatr Nephrol; 2007 Nov; 22(11):1975-8. PubMed ID: 17680274
[TBL] [Abstract][Full Text] [Related]
4. Oral self-mutilation by a 17-month-old child with Lesch-Nyhan syndrome.
Rashid N; Yusuf H
Int J Paediatr Dent; 1997 Jun; 7(2):115-7. PubMed ID: 9524464
[TBL] [Abstract][Full Text] [Related]
5. Oral self-mutilation in the Lesch-Nyhan syndrome.
Lee JH; Berkowitz RJ; Choi BJ
ASDC J Dent Child; 2002; 69(1):66-9, 12. PubMed ID: 12119817
[TBL] [Abstract][Full Text] [Related]
6. A preventive approach to oral self-mutilation in Lesch-Nyhan syndrome: a case report.
Jeong TS; Lee JH; Kim S; Kim JH; Tootla RG
Pediatr Dent; 2006; 28(4):341-4. PubMed ID: 16903443
[TBL] [Abstract][Full Text] [Related]
7. Late diagnosis of Lesch-Nyhan disease complicated with end-stage renal disease and tophi burst: a case report.
Ambarsari CG; Cahyadi D; Sari L; Satria O; Sahli F; Darmadi TL; Kadaristiana A
Ren Fail; 2020 Nov; 42(1):113-121. PubMed ID: 31985336
[No Abstract] [Full Text] [Related]
8. The Lesch-Nyhan syndrome--an under-recognised condition in South Africa? A case report.
Gilbert RD; Wiggelinkhuizen J; Harley EH; Marinaki A
S Afr Med J; 1992 Apr; 81(7):375-7. PubMed ID: 1561565
[TBL] [Abstract][Full Text] [Related]
9. Self-mutilation behaviour in Lesch-Nyhan syndrome.
Cauwels RG; Martens LC
J Oral Pathol Med; 2005 Oct; 34(9):573-5. PubMed ID: 16138897
[TBL] [Abstract][Full Text] [Related]
10. Lesch-Nyhan syndrome due to a splice-site mutation in a 14-month-old boy presenting as acute renal failure.
Kollios K; Savvidou P; Karipiadou A; Zagkanika S; Seitanidou S; Vargiami E; Zafeiriou D; Roilides E
Clin Nephrol; 2021 Aug; 96(2):120-123. PubMed ID: 33993907
[TBL] [Abstract][Full Text] [Related]
11. Lesch-Nyhan syndrome: surgical treatment in a case with lip chewing. A case report.
LaBanc J; Epker BN
J Maxillofac Surg; 1981 Feb; 9(1):64-7. PubMed ID: 6939776
[TBL] [Abstract][Full Text] [Related]
12. Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature.
Vargiami E; Printza N; Papadimiditriou E; Batzios S; Kyriazi M; Papachristou F; Zafeiriou DI
Urology; 2016 Nov; 97():194-196. PubMed ID: 27079129
[TBL] [Abstract][Full Text] [Related]
13. Lesch-Nyhan syndrome presenting as acute renal failure secondary to obstructive uropathy.
Ankem M; Glazier DB; Barone JG
Urology; 2000 Dec; 56(6):1056. PubMed ID: 11113762
[TBL] [Abstract][Full Text] [Related]
14. Botulinum toxin as a novel treatment for self-mutilation in Lesch-Nyhan syndrome.
Dabrowski E; Smathers SA; Ralstrom CS; Nigro MA; Leleszi JP
Dev Med Child Neurol; 2005 Sep; 47(9):636-9. PubMed ID: 16138673
[TBL] [Abstract][Full Text] [Related]
15. Differential diagnosis of cerebral palsy: Lesch-Nyhan syndrome without self-mutilation.
Mitchell G; McInnes RR
Can Med Assoc J; 1984 May; 130(10):1323-4. PubMed ID: 6722697
[TBL] [Abstract][Full Text] [Related]
16. Xanthine calculi in a patient with Lesch-Nyhan syndrome and factor V Leiden treated with allopurinol: case report.
Shields LBE; Peppas DS; Rosenberg E
BMC Pediatr; 2018 Jul; 18(1):231. PubMed ID: 30001695
[TBL] [Abstract][Full Text] [Related]
17. Lesch-Nyhan Syndrome: report on two brothers.
Yang MT; Mak SC; Chi CS; Lin HY; Lii YP; Wu KH; Shian WJ
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(6):552-8. PubMed ID: 7831990
[TBL] [Abstract][Full Text] [Related]
18. [Neurologic and psychiatric aspects of Lesch-Nyhan syndrome].
Heidelmann G; Knauthe M
Psychiatr Neurol Med Psychol (Leipz); 1982 Feb; 34(2):79-87. PubMed ID: 7089122
[TBL] [Abstract][Full Text] [Related]
19. [A Japanese family with Lesch-Nyhan syndrome resulting from a new point mutation in hypoxanthine-guanine phosphoribosyltransferase gene].
Maruta K; Ohi T; Yamada Y; Goto H; Ogasawara N; Matsukura S
No To Shinkei; 1997 Nov; 49(11):1009-13. PubMed ID: 9396032
[TBL] [Abstract][Full Text] [Related]
20. Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants).
Seegmiller JE
Adv Hum Genet; 1976; 6():75-163. PubMed ID: 779428
[No Abstract] [Full Text] [Related]
[Next] [New Search]