163 related articles for article (PubMed ID: 16684290)
1. Oculocutaneous tyrosinaemia or tyrosinaemia type 2: a case report.
Valikhani M; Akhyani M; Jafari AK; Barzegari M; Toosi S
J Eur Acad Dermatol Venereol; 2006 May; 20(5):591-4. PubMed ID: 16684290
[TBL] [Abstract][Full Text] [Related]
2. [Oculocutaneous type II tyrosinosis].
Podglajen-Wecxsteen O; Delaporte E; Piette F; le Flohic X; Bergoend H
Ann Dermatol Venereol; 1993; 120(2):139-42. PubMed ID: 8363306
[TBL] [Abstract][Full Text] [Related]
3. [Tyrosinemia type II. Case report].
Benatiya AI; Bouayed MA; Touiza E; Daoudi K; Bhalil S; Elmesbahi I; Tahri H
Bull Soc Belge Ophtalmol; 2005; (296):57-61. PubMed ID: 16050420
[TBL] [Abstract][Full Text] [Related]
4. Richner-Hanhart syndrome (tyrosinemia type II): a case report of delayed diagnosis with pseudodendritic corneal lesion.
Iskeleli G; Bilgeç MD; Arici C; Atalay E; Oğreden T; Aydin A
Turk J Pediatr; 2011; 53(6):692-4. PubMed ID: 22389994
[TBL] [Abstract][Full Text] [Related]
5. Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic response.
al-Essa MA; Rashed MS; Ozand PT
East Mediterr Health J; 1999 Nov; 5(6):1204-7. PubMed ID: 11924112
[TBL] [Abstract][Full Text] [Related]
6. Richner-Hanhart syndrome (tyrosinemia II): early diagnosis of an incomplete presentation with unusual findings.
Viglizzo GM; Occella C; Bleidl D; Rongioletti F
Pediatr Dermatol; 2006; 23(3):259-61. PubMed ID: 16780475
[TBL] [Abstract][Full Text] [Related]
7. [Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet].
Ogier H; Hervé F; Saudubray JM; Dufier JL; Charpentier C; Lemonnier F; Moreno JL; Frezal J
Ann Med Interne (Paris); 1986; 137(2):129-32. PubMed ID: 2940955
[TBL] [Abstract][Full Text] [Related]
8. Tyrosinaemia type II with diffuse plantar keratoderma and self-mutilation.
Madan V; Gupta U
Clin Exp Dermatol; 2006 Jan; 31(1):54-6. PubMed ID: 16309482
[TBL] [Abstract][Full Text] [Related]
9. [Two cases of Richner-Hanhart syndrome (oculocutaneous tyrosinemia)].
Bygum A; Brandrup F; Gade EF; Lund AM; Christensen E
Ugeskr Laeger; 2008 Feb; 170(8):655. PubMed ID: 18364160
[TBL] [Abstract][Full Text] [Related]
10. Richner-Hanhart syndrome detected by expanded newborn screening.
Meissner T; Betz RC; Pasternack SM; Eigelshoven S; Ruzicka T; Kruse R; Laitenberger G; Mayatepek E
Pediatr Dermatol; 2008; 25(3):378-80. PubMed ID: 18577048
[TBL] [Abstract][Full Text] [Related]
11. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome.
Soares DC; Stroparo MN; Lian YC; Takakura CY; Wolf S; Betz R; Kim CA
J Inherit Metab Dis; 2017 May; 40(3):461-462. PubMed ID: 27832414
[TBL] [Abstract][Full Text] [Related]
12. [Oculo-cutaneous tyrosinosis (Richner-Hanhart syndrome). Histo-pathological study of a case].
Larregue M; de Giacomoni P; Odievre M; Babin P; Lorette G
Ann Anat Pathol (Paris); 1980; 25(3):185-200. PubMed ID: 6112939
[TBL] [Abstract][Full Text] [Related]
13. Tyrosinemia type II: nine cases of ocular signs and symptoms.
Macsai MS; Schwartz TL; Hinkle D; Hummel MB; Mulhern MG; Rootman D
Am J Ophthalmol; 2001 Oct; 132(4):522-7. PubMed ID: 11589874
[TBL] [Abstract][Full Text] [Related]
14. [Richner-Hanhart's syndrome or oculo-cutaneous tyrosinosis (about one case) (author's transl)].
Larrègue M; de Giacomoni P; Bressieux JM; Odièvre M
Ann Dermatol Venereol; 1979 Jan; 106(1):53-62. PubMed ID: 485016
[TBL] [Abstract][Full Text] [Related]
15. TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.
Maydan G; Andresen BS; Madsen PP; Zeigler M; Raas-Rothschild A; Zlotogorski A; Gutman A; Korman SH
J Inherit Metab Dis; 2006 Oct; 29(5):620-6. PubMed ID: 16917729
[TBL] [Abstract][Full Text] [Related]
16. The genetic tyrosinemias.
Scott CR
Am J Med Genet C Semin Med Genet; 2006 May; 142C(2):121-6. PubMed ID: 16602095
[TBL] [Abstract][Full Text] [Related]
17. [Changes in the keratinocytes in oculo-cutaneous tyrosinosis: Richner-Hanhart syndrome (author's transl)].
Larrègue M; De Giacomoni P; Odièvre P; Prigent F
Ann Dermatol Venereol; 1980; 107(11):1023-30. PubMed ID: 7235483
[TBL] [Abstract][Full Text] [Related]
18. Two siblings with tyrosinaemia type 2.
Aydin OF; Zorlu P; Kunak B; Tezic T; Eken A
Eur J Pediatr; 2003 Feb; 162(2):81-3. PubMed ID: 12548382
[TBL] [Abstract][Full Text] [Related]
19. Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.
Bouyacoub Y; Zribi H; Azzouz H; Nasrallah F; Abdelaziz RB; Kacem M; Rekaya B; Messaoud O; Romdhane L; Charfeddine C; Bouziri M; Bouziri S; Tebib N; Mokni M; Kaabachi N; Boubaker S; Abdelhak S
Gene; 2013 Oct; 529(1):45-9. PubMed ID: 23954227
[TBL] [Abstract][Full Text] [Related]
20. Unusual dendritic keratitis.
Gokhale NS; Dherai AJ; Desai H; Ashavaid TF
Indian J Ophthalmol; 2007; 55(1):57-9. PubMed ID: 17189889
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]