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Journal Abstract Search

112 related items for PubMed ID: 3402627

  • 21. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N, Jordaan FH, Taljaard JJ, Hough SF.
    Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
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  • 23. [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
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  • 25. Advanced Coats' disease.
    Haik BG.
    Trans Am Ophthalmol Soc; 1991 Oct; 89():371-476. PubMed ID: 1808814
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  • 27. Coats' disease and congenital vascular retinopathy.
    Campbell FP.
    Trans Am Ophthalmol Soc; 1976 Oct; 74():365-424. PubMed ID: 325857
    [No Abstract] [Full Text] [Related]

  • 28. [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].
    Mende B, Kreysel HW.
    Hautarzt; 1987 Sep; 38(9):532-5. PubMed ID: 3692855
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  • 29. Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
    Ibsen HH, Clemmensen OJ, Brandrup F.
    Acta Derm Venereol; 1991 Sep; 71(4):349-51. PubMed ID: 1681656
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  • 31. [Fungi, psychological aspects, immune system.... Why is the child loosing hair?].
    Paukstadt W.
    MMW Fortschr Med; 2001 Sep 27; 143(39):10-2. PubMed ID: 11680920
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  • 32. [Familial congenital hypotrichosis with "uncombable hair," retinal pigmentary dystrophy, juvenile cataract and brachymetacarpia: another entity of the ectodermal dysplasia group].
    Bork K, Stender E, Schmidt D, Berzas C, Rochels R.
    Hautarzt; 1987 Jun 27; 38(6):342-7. PubMed ID: 3654205
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  • 33. Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.
    Castori M, Ruggieri S, Giannetti L, Annessi G, Zambruno G.
    Acta Derm Venereol; 2008 Jun 27; 88(6):607-12. PubMed ID: 19002348
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  • 34.
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  • 35. Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
    Naz G, Khan B, Ali G, Azeem Z, Wali A, Ansar M, Ahmad W.
    J Dermatol Sci; 2009 Apr 27; 54(1):12-6. PubMed ID: 19167195
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  • 36. Heritable disorders of hair.
    Birnbaum PS, Baden HP.
    Dermatol Clin; 1987 Jan 27; 5(1):137-53. PubMed ID: 3549074
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  • 37. Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification.
    Slee J, Lam G, Walpole I.
    Am J Med Genet; 1999 Jun 04; 84(4):330-3. PubMed ID: 10340646
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  • 38. Coats' disease diagnosed in adulthood.
    Smithen LM, Brown GC, Brucker AJ, Yannuzzi LA, Klais CM, Spaide RF.
    Ophthalmology; 2005 Jun 04; 112(6):1072-8. PubMed ID: 15882905
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  • 39. [Loose anagen hair syndrome: a familial case with fetal hair in meconium].
    Khadir K, Habibeddine S, Azzouzi S, Lakhdar H, Van Neste D.
    Ann Dermatol Venereol; 2001 Jan 04; 128(1):52-4. PubMed ID: 11226903
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  • 40. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
    Lefevre P, Rochat A, Bodemer C, Vabres P, Barrandon Y, de Prost Y, Garner C, Hovnanian A.
    Eur J Hum Genet; 2000 Apr 04; 8(4):273-9. PubMed ID: 10854110
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