BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 17389849)

  • 1. [Collodion baby with neonatal signs of trichothiodystrophy misdiagnosed as Netherton syndrome: reassessment of a previous diagnostic error].
    Larrègue M; Guillet G
    Ann Dermatol Venereol; 2007 Mar; 134(3 Pt 1):245-8. PubMed ID: 17389849
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Trichothiodystrophy: progresssive manifestations].
    Foulc P; Jumbou O; David A; Sarasin A; Stalder JF
    Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Collodion baby: 32 new case reports].
    Larrègue M; Ottavy N; Bressieux JM; Lorette J
    Ann Dermatol Venereol; 1986; 113(9):773-85. PubMed ID: 3548541
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Netherton syndrome associated with idiopathic congenital hemihypertrophy.
    Yerebakan O; Uğuz A; Keser I; Lüleci G; Ciftçioğlu MA; Başaran E; Alpsoy E
    Pediatr Dermatol; 2002; 19(4):345-8. PubMed ID: 12220283
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Collodion baby. Clinical course based on 29 cases].
    Larrègue M; Gharbi R; Daniel J; Le Marec Y; Civatte J
    Ann Dermatol Syphiligr (Paris); 1976; 103(1):31-56. PubMed ID: 793506
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ichthyosis with confetti: clinics, molecular genetics and management.
    Guerra L; Diociaiuti A; El Hachem M; Castiglia D; Zambruno G
    Orphanet J Rare Dis; 2015 Sep; 10():115. PubMed ID: 26381864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome.
    Sprecher E; Tesfaye-Kedjela A; Ratajczak P; Bergman R; Richard G
    Clin Exp Dermatol; 2004 Sep; 29(5):513-7. PubMed ID: 15347338
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Trichothiodystrophy].
    Meynadier J; Guillot B; Barnéon G; Djian B; Lévy A
    Ann Dermatol Venereol; 1987; 114(12):1529-36. PubMed ID: 3445983
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Severe hypernatremic dehydration in an infant with Netherton syndrome.
    Stoll C; Alembik Y; Tchomakov D; Messer J; Heid E; Boehm N; Calvas P; Hovnanian A
    Genet Couns; 2001; 12(3):237-43. PubMed ID: 11693786
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Trichothiodystrophy and congenital heart disease in two sisters].
    Mazereeuw-Hautier J; Pech JH; Heitz F; Bonafe JL
    Ann Dermatol Venereol; 2002 Oct; 129(10 Pt 1):1168-71. PubMed ID: 12442133
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Development of a disease severity score for newborns with collodion membrane.
    Rubio-Gomez GA; Weinstein M; Pope E
    J Am Acad Dermatol; 2014 Mar; 70(3):506-11. PubMed ID: 24373778
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype.
    Anker P; Kiss N; Kocsis I; Czemmel É; Becker K; Zakariás S; Plázár D; Farkas K; Mayer B; Nagy N; Széll M; Ács N; Szalai Z; Medvecz M
    Life (Basel); 2021 Jun; 11(7):. PubMed ID: 34199106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inherited ichthyosis: Syndromic forms.
    Yoneda K
    J Dermatol; 2016 Mar; 43(3):252-63. PubMed ID: 26945533
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Case report of self-improving collodion ichthyosis in the newborn.
    Zhu S; Jiang Y; Shen N; Yin H; Qiao J
    J Int Med Res; 2023 Oct; 51(10):3000605231204491. PubMed ID: 37848341
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Collodion baby and respiratory distress syndrome].
    Loumouamou Y; Boumahni B; Kauffmann E; Randrianaivo H; Jacquemont ML
    J Gynecol Obstet Biol Reprod (Paris); 2012 Feb; 41(1):88-91. PubMed ID: 21733637
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome.
    Hausser I; Anton-Lamprecht I
    Pediatr Dermatol; 1996; 13(3):183-99. PubMed ID: 8806118
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Collodion Baby with TGM1 gene mutation.
    Sharma D; Gupta B; Shastri S; Pandita A; Pawar S
    Int Med Case Rep J; 2015; 8():205-8. PubMed ID: 26451124
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Collodion baby. Apropos of a case with eye manifestations].
    Algan M; Bouhanna A; Gaudric A; Elbez A; Canet J; Coscas G
    J Fr Ophtalmol; 1989; 12(5):399-402. PubMed ID: 2621312
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Collodion baby: clinical aspects and role of prenatal diagnosis].
    Fatnassi R; Marouen N; Ragmoun H; Marzougui L; Hammami S
    Pan Afr Med J; 2017; 26():118. PubMed ID: 28533841
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Collodion baby concomitant with congenital hypothyroidism: a patient report and review of the literature.
    Kurtoğlu S; Caksen H; Erdoğan R; Kisaarslan AF
    J Pediatr Endocrinol Metab; 1998; 11(4):569-73. PubMed ID: 9777579
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.