BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 2062544)

  • 1. Sjögren-Larsson syndrome: case reports of two brothers.
    Barnard NA; Patel C; Barnard RA
    Ophthalmic Physiol Opt; 1991 Apr; 11(2):180-3. PubMed ID: 2062544
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A very rare neurocutaneous disorder in 2 siblings: Sjögren-Larsson syndrome.
    Caglayan AO; Gumus H
    J Child Neurol; 2010 Aug; 25(8):1003-5. PubMed ID: 20142464
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Patients with Sjögren-Larsson syndrome lack macular pigment.
    van der Veen RL; Fuijkschot J; Willemsen MA; Cruysberg JR; Berendschot TT; Theelen T
    Ophthalmology; 2010 May; 117(5):966-71. PubMed ID: 20163870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sjögren-Larsson syndrome.
    Rizzo WB
    Semin Dermatol; 1993 Sep; 12(3):210-8. PubMed ID: 8217559
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sjögren-Larsson syndrome: a case report and literature review.
    Alió AB; Bird LM; McClellan SD; Cunningham BB
    Cutis; 2006 Jul; 78(1):61-5. PubMed ID: 16903323
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Incomplete Sjögren-Larsson syndrome in two Japanese siblings.
    Kawakami T; Saito R; Fujikawa Y; Kazama H; Shinomiya N; Yamaguchi K; Yamaguchi Y; Aoki T; Kobayashi T
    Dermatology; 1999; 198(1):93-6. PubMed ID: 10026413
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosing Sjögren-Larsson syndrome in a 7-year-old Moroccan boy.
    Bernardini ML; Cangiotti AM; Zamponi N; Porfiri L; Cinti S; Offidani A
    J Cutan Pathol; 2007 Mar; 34(3):270-5. PubMed ID: 17302612
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sjogren-larsson syndrome: case report and review of neurologic abnormalities and ichthyosis.
    Dutra LA; de Aquino CC; Barsottini OG
    Neurologist; 2009 Nov; 15(6):332-4. PubMed ID: 19901712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sjogren-Larsson Syndrome: A case series of five members from an extended family with a novel mutation.
    Abidi KT; Kamal NM; Bakkar A AA; Alotaibi M; Asseri H; Bokari KA
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1487. PubMed ID: 32930514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.
    Pigg M; Annton-Lamprecht I; Braun-Quentin C; Gustavson KH; Wadelius C
    Acta Derm Venereol; 1999 Jan; 79(1):41-3. PubMed ID: 10086857
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical, biochemical, and genetic aspects of Sjögren-Larsson syndrome.
    Cho KH; Shim SH; Kim M
    Clin Genet; 2018 Apr; 93(4):721-730. PubMed ID: 28543186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sjögren-Larsson syndrome.
    Der Kinderen DJ; Cruysberg JR; Steijlen PM
    Br J Dermatol; 1993 Aug; 129(2):213-4. PubMed ID: 7654590
    [No Abstract]   [Full Text] [Related]  

  • 13. Sjögren-Larsson syndrome: optical coherence tomography and a novel mutation.
    Burgueño-Montañés C; García-Fernández M; Colunga-Cueva M; García-López A
    Arch Soc Esp Oftalmol; 2014 Dec; 89(12):504-7. PubMed ID: 24377952
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Sjögren-Larsson syndrome: Pediatric case report].
    García-Ortiz L; Gómez-López R; Rivera-Pedroza CI; Santillán-Hernández Y; Chima-Galán MDC; Gutiérrez-Salinas J
    Arch Argent Pediatr; 2018 Dec; 116(6):e773-e777. PubMed ID: 30457735
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sjögren-Larsson syndrome: case reports.
    Levisohn D; Dintiman B; Rizzo WB
    Pediatr Dermatol; 1991 Sep; 8(3):217-20. PubMed ID: 1836061
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Macular crystalline dystrophy in Sjögren-Larsson syndrome: case report].
    Isaac DL; Queiroz GH; Feres CC; Avila M
    Arq Bras Oftalmol; 2009; 72(2):239-42. PubMed ID: 19466337
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sjögren-Larsson syndrome: a rare disease of the skin and central nervous system.
    Roy U; Das U; Pandit A; Debnath A
    BMJ Case Rep; 2016 Apr; 2016():10.1136/bcr-2016-215110. PubMed ID: 27095813
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sjögren-Larsson syndrome: novel mutations in the ALDH3A2 gene in a French cohort.
    Sarret C; Rigal M; Vaurs-Barrière C; Dorboz I; Eymard-Pierre E; Combes P; Giraud G; Wanders RJ; Afenjar A; Francannet C; Boespflug-Tanguy O
    J Neurol Sci; 2012 Jan; 312(1-2):123-6. PubMed ID: 21872273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. First prenatal diagnosis by mutation analysis in a family with Sjögren-Larsson syndrome.
    Sillén A; Holmgren G; Wadelius C
    Prenat Diagn; 1997 Dec; 17(12):1147-9. PubMed ID: 9467812
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Update on Sjögren-Larsson syndrome.
    Lacour M
    Dermatology; 1996; 193(2):77-82. PubMed ID: 8884139
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.