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 *

83 related articles for article (PubMed ID: 7654590)

  • 21. The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic association.
    Pigg M; Jagell S; Sillén A; Weissenbach J; Gustavson KH; Wadelius C
    Nat Genet; 1994 Dec; 8(4):361-4. PubMed ID: 7894487
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Sjogren-Larsson syndrome.
    Phanthumchinda K; Srimanuthipol K; Yodnophaklao P
    J Med Assoc Thai; 1996 Aug; 79(8):541-4. PubMed ID: 8855639
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Sjögren-Larsson syndrome due to a novel mutation in the FALDH gene.
    Botelho Gomes JM; Vieira AP; Navarro J; Maré R; Tavares P; Brito C
    Eur J Dermatol; 2011; 21(3):412-3. PubMed ID: 21524986
    [No Abstract]   [Full Text] [Related]  

  • 24. Topical treatment of CHILD nevus and Sjögren-Larsson Syndrome with combined lovastatin and cholesterol.
    Merino De Paz N; Rodriguez-Martin M; Contreras-Ferrer P; Garcia Bustinduy M; Gonzalez Perera I; Virgos Aller T; Martin Herrera A; Noda Cabrera A
    Eur J Dermatol; 2011; 21(6):1026-7. PubMed ID: 21983059
    [No Abstract]   [Full Text] [Related]  

  • 25. Sjögren-Larsson syndrome: biochemical defects and follow up in three cases.
    Auada MP; Taube MB; Collares EF; Tanaka AM; Cintra ML
    Eur J Dermatol; 2002; 12(3):263-6. PubMed ID: 11978568
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene.
    De Laurenzi V; Rogers GR; Hamrock DJ; Marekov LN; Steinert PM; Compton JG; Markova N; Rizzo WB
    Nat Genet; 1996 Jan; 12(1):52-7. PubMed ID: 8528251
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. A case of Sjögren-Larsson syndrome.
    Sarìcaoglu H; Tunalì S; Bülbül E; Alpakut S; Ozmen AT; Okan M; Palalì Z
    J Eur Acad Dermatol Venereol; 1999 Jan; 12(1):76-8. PubMed ID: 10188163
    [No Abstract]   [Full Text] [Related]  

  • 29. Sjögren-larsson syndrome and crystalline maculopathy associated with a novel mutation.
    Jean-François E; Low JY; Gonzales CR; Sarraf D
    Arch Ophthalmol; 2007 Nov; 125(11):1582-3. PubMed ID: 17998529
    [No Abstract]   [Full Text] [Related]  

  • 30. Sjögren-Larsson syndrome: nuclear magnetic resonance imaging of the brain in a 4-year-old boy.
    Di Rocco M; Filocamo M; Tortori-Donati P; Veneselli E; Borrone C; Rizzo WB
    J Inherit Metab Dis; 1994; 17(1):112-4. PubMed ID: 8051916
    [No Abstract]   [Full Text] [Related]  

  • 31. Dystonia secondary to Sjögren-Larsson syndrome.
    Cubo E; Goetz CG
    Neurology; 2000 Oct; 55(8):1236-7. PubMed ID: 11071513
    [No Abstract]   [Full Text] [Related]  

  • 32. A novel point mutation of the FALDH gene in a Japanese family with Sjögren-Larsson syndrome.
    Aoki N; Suzuki H; Ito K; Ito M
    J Invest Dermatol; 2000 May; 114(5):1065-6. PubMed ID: 10792573
    [No Abstract]   [Full Text] [Related]  

  • 33. [Sjögren-Larsson syndrome].
    Kubota T
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):646-7. PubMed ID: 11528943
    [No Abstract]   [Full Text] [Related]  

  • 34. Cerebral MRI and spectroscopy in Sjögren-Larsson syndrome: case report.
    Miyanomae Y; Ochi M; Yoshioka H; Takaya K; Kizaki Z; Inoue F; Furuya S; Naruse S
    Neuroradiology; 1995 Apr; 37(3):225-8. PubMed ID: 7603599
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Enzymatic diagnosis of Sjögren-Larsson syndrome using electrospray ionization mass spectrometry.
    Sanders RJ; Ofman R; Dekker C; Kemp S; Wanders RJ
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Feb; 877(4):451-5. PubMed ID: 19124283
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjögren-Larsson syndrome.
    Willemsen MA; Steijlen PM; de Jong JG; Rotteveel JJ; IJlst L; van Werkhoven MA; Wanders RJ
    J Invest Dermatol; 1999 May; 112(5):827-8. PubMed ID: 10233781
    [No Abstract]   [Full Text] [Related]  

  • 37. [Sjögren Larsson syndrome].
    Reich H
    Med Klin; 1972 Jun; 67(26):909-12. PubMed ID: 5048685
    [No Abstract]   [Full Text] [Related]  

  • 38. Detection of hexanol dehydrogenase activity in the epidermis of a patient with Sjögren-Larsson syndrome.
    Yasaka N; Fujimoto M; Tamaki K
    J Dermatol; 1992 Apr; 19(4):258-9. PubMed ID: 1607492
    [No Abstract]   [Full Text] [Related]  

  • 39. Expanding the Genotype of Sjögren-Larsson Syndrome: A New Case Due to Two Novel Mutations.
    García-Peris E; Latour-Álvarez I; Pestana-Eliche M; Sánchez R
    Actas Dermosifiliogr; 2017; 108(6):601-603. PubMed ID: 28410621
    [No Abstract]   [Full Text] [Related]  

  • 40. [A new mutation in the ALDH3A2 gene in a boy with Sjogren-Larsson syndrome].
    Mora-Lopez F; Vilches-Moreno M; Marin-Iglesias R
    Rev Neurol; 2018 Nov; 67(10):415-416. PubMed ID: 30403285
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.