BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 4462624)

  • 1. Cutis laxa-a heterogeneous disorder.
    Beighton P
    Birth Defects Orig Artic Ser; 1974; 10(10):126-31. PubMed ID: 4462624
    [No Abstract]   [Full Text] [Related]  

  • 2. Cutis laxa, intrauterine growth retardation, and bilateral dislocation of the hips: a report of five cases.
    Karrar ZA; Elidrissy AT; Adam KA
    Prog Clin Biol Res; 1982; 104():215-22. PubMed ID: 6891788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cutis laxa of the autosomal recessive type in a consanguineous family.
    de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
    Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
    Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
    Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Defective protein glycosylation in patients with cutis laxa syndrome.
    Morava E; Wopereis S; Coucke P; Gillessen-Kaesbach G; Voit T; Smeitink J; Wevers R; Grünewald S
    Eur J Hum Genet; 2005 Apr; 13(4):414-21. PubMed ID: 15657616
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cutis laxa. Classification, clinical aspects and molecular defects].
    Mensing H; Krieg T; Meigel W; Braun-Falco O
    Hautarzt; 1984 Oct; 35(10):506-11. PubMed ID: 6500933
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn.
    Koklu E; Gunes T; Ozturk MA; Akcakus M; Buyukkayhan D; Kurtoglu S
    Pediatr Dermatol; 2007; 24(5):525-8. PubMed ID: 17958802
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibs.
    Van Maldergem L; Vamos E; Liebaers I; Petit P; Vandevelde G; Simonis-Blumenfrucht A; Bouffioux R; Kulakowski S; Hanquinet S; Van Durme P
    Am J Med Genet; 1988 Oct; 31(2):455-64. PubMed ID: 3232707
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cutis laxa syndrome. Clinical, histologic and ultrastructural study of a new variant].
    Pitzalis G; Bonamico M; Mariani P; Palmieri G; Ceccamea A; Signoretti A
    Minerva Pediatr; 1989 Apr; 41(4):193-7. PubMed ID: 2770644
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cardiovascular changes in the cutis laxa congenita syndrome].
    Guía Torrent JM; Castro García F; Cuenca Gómez M; Gracián Gómez M
    Rev Esp Cardiol; 1999 Mar; 52(3):204-6. PubMed ID: 10193176
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital cutis laxa with a dominant inheritance and early onset emphysema.
    Corbett E; Glaisyer H; Chan C; Madden B; Khaghani A; Yacoub M
    Thorax; 1994 Aug; 49(8):836-7. PubMed ID: 8091333
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital cutis laxa syndrome: type II autosomal recessive inheritance.
    Tüysüz B; Arapoğlu M; Ilikkan B; Demirkesen C; Perk Y
    Turk J Pediatr; 2003; 45(3):265-8. PubMed ID: 14696810
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital cutis laxa with retardation of growth and development.
    Patton MA; Tolmie J; Ruthnum P; Bamforth S; Baraitser M; Pembrey M
    J Med Genet; 1987 Sep; 24(9):556-61. PubMed ID: 3669050
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The dominant and recessive forms of cutis laxa.
    Beighton P
    J Med Genet; 1972 Jun; 9(2):216-21. PubMed ID: 5046633
    [No Abstract]   [Full Text] [Related]  

  • 15. [Concomitance and significance of cutis laxa and infantile alveolar pulmonary emphysema in an unusual anatomopathological case].
    Bondi R; Gori F; Treves G
    Arch De Vecchi Anat Patol; 1968 Jul; 51(3):801-20. PubMed ID: 5738240
    [No Abstract]   [Full Text] [Related]  

  • 16. [Congenital generalized cutis laxa: 5 cases].
    Rybojad M; Baumann C; Godeau G; Moraillon I; Prigent F; Morel P; Bourrat E
    Ann Dermatol Venereol; 1999 Apr; 126(4):317-9. PubMed ID: 10421933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Congenital cutis laxa. A case report with an electron microscopic study].
    Sauviat C; Durepaire RM; Cesarini JP; Borde M
    Ann Pediatr (Paris); 1978 Sep; 25(7):355-61. PubMed ID: 16114347
    [No Abstract]   [Full Text] [Related]  

  • 18. Decreased bone density and treatment in patients with autosomal recessive cutis laxa.
    Noordam C; Funke S; Knoers NV; Jira P; Wevers RA; Urban Z; Morava E
    Acta Paediatr; 2009 Mar; 98(3):490-4. PubMed ID: 19055655
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in PYCR1 gene in three families with autosomal recessive cutis laxa, type 2.
    Scherrer DZ; Baptista MB; Matos AH; Maurer-Morelli CV; Steiner CE
    Eur J Med Genet; 2013 Jun; 56(6):336-9. PubMed ID: 23531708
    [No Abstract]   [Full Text] [Related]  

  • 20. [Generalized congenital cutis laxa associated with visceral lesions].
    Bechelli LM; Pagnano PM; De Souza NM; Soares LM; Rossi MA; Marin Neto JA; Arevalo JR; Trad ES; Maciel BC
    Ann Dermatol Venereol; 1985; 112(10):835-9. PubMed ID: 4091409
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.