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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 36118278)

  • 1. A child with dendritiform eye lesions and developmental delay.
    Gliagias V; Denisova K; Kang JJ
    Am J Ophthalmol Case Rep; 2022 Dec; 28():101701. PubMed ID: 36118278
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Corneal lesion as the initial manifestation of tyrosinemia type II.
    Tsai CP; Lin PY; Lee NC; Niu DM; Lee SM; Hsu WM
    J Chin Med Assoc; 2006 Jun; 69(6):286-8. PubMed ID: 16863017
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Richner-Hanhart syndrome and tyrosinemia type II.
    Hunziker N
    Dermatologica; 1980; 160(3):180-9. PubMed ID: 6446465
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. Pseudodendritic keratitis and systemic tyrosinemia.
    Charlton KH; Binder PS; Wozniak L; Digby DJ
    Ophthalmology; 1981 Apr; 88(4):355-60. PubMed ID: 6454871
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review.
    al-Hemidan AI; al-Hazzaa SA
    Ophthalmic Genet; 1995 Mar; 16(1):21-6. PubMed ID: 7648039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. In vivo confocal microscopic features of corneal pseudodendritic lesions in tyrosinemia type II.
    Kocabeyoglu S; Mocan MC; Irkec M
    Cornea; 2014 Oct; 33(10):1106-8. PubMed ID: 25119963
    [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. [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]  

  • 12. An Infant with Bilateral Keratitis: From Infectious to Genetic Diagnosis.
    Thibault LP; Mitchell GA; Parisien B; Hamel P; Blanchard AC
    Am J Case Rep; 2022 Nov; 23():e937967. PubMed ID: 36447403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Herpetiform bilateral epithelial corneal dystrophy caused by Tyrosinemia (Richner-Hanhart-Syndrome) (author's transl)].
    Jaeger W; Gallasch G; Schnyder UW; Lutz P; Schmidt H
    Klin Monbl Augenheilkd; 1978 Oct; 173(4):506-15. PubMed ID: 153427
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Corneal Pseudodendritic Lesions Masquerading as Herpetic Keratitis in a Patient With Tyrosinemia Type I.
    Gulmez Sevim D; Gumus K; Cavanagh HD
    Eye Contact Lens; 2017 May; 43(3):e7-e9. PubMed ID: 26322918
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Painful keratoderma and photophobia: hallmarks of tyrosinemia type II.
    Rabinowitz LG; Williams LR; Anderson CE; Mazur A; Kaplan P
    J Pediatr; 1995 Feb; 126(2):266-9. PubMed ID: 7844676
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene.
    Culic V; Betz RC; Refke M; Fumic K; Pavelic J
    Eur J Med Genet; 2011; 54(3):205-8. PubMed ID: 21145993
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tyrosinemia type II in two cases previously reported as Richner-Hanhart syndrome.
    Balato N; Cusano F; Lembo G; Santoianni P
    Dermatologica; 1986; 173(2):66-74. PubMed ID: 2947825
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.