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Items: 1 to 20 of 29

1.

The Tay syndrome (congenital ichthyosis with trichothiodystrophy).

Happle R, Traupe H, Gröbe H, Bonsmann G.

Eur J Pediatr. 1984 Jan;141(3):147-52.

PMID:
6538137
2.

Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay syndrome.

Lambert WC, Gagna CE, Lambert MW.

Adv Exp Med Biol. 2010;685:106-10. Review.

PMID:
20687499
3.

Tay or IBIDS syndrome. A case with growth and mental retardation, congenital ichthyosis and brittle hair.

Blomquist HK, Bäck O, Fagerlund M, Holmgren G, Stecksén-Blicks C.

Acta Paediatr Scand. 1991 Dec;80(12):1241-5. Review.

PMID:
1785299
4.

[Netherton's syndrome. Current aspects. Apropos of 9 cases].

Plantin P, Delaire P, Guillet MH, Labouche F, Guillet G.

Ann Dermatol Venereol. 1991;118(8):525-30. Review. French.

PMID:
1952689
5.

Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias.

Itin PH, Pittelkow MR.

J Am Acad Dermatol. 1990 May;22(5 Pt 1):705-17. Review.

PMID:
2189905
6.

Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature.

Civitelli R, McAlister WH, Teitelbaum SL, Whyte MP.

J Bone Miner Res. 1989 Dec;4(6):863-75. Review.

PMID:
2692405
7.

PIBI(D)S: clinical and molecular characterization of a new case.

Fortina AB, Alaibac M, Piaserico S, Peserico A.

J Eur Acad Dermatol Venereol. 2001 Jan;15(1):65-9. Review.

PMID:
11451329
8.

Ichthyosis: etiology, diagnosis, and management.

DiGiovanna JJ, Robinson-Bostom L.

Am J Clin Dermatol. 2003;4(2):81-95. Review.

PMID:
12553849
9.

[What is new in genetically-induced hair diseases?].

Traupe H, Hamm H.

Z Hautkr. 1990 Dec;65(12):1085-91. Review. German.

PMID:
2087835
10.

New clinico-genetic classification of trichothiodystrophy.

Morice-Picard F, Cario-André M, Rezvani H, Lacombe D, Sarasin A, Taïeb A.

Am J Med Genet A. 2009 Sep;149A(9):2020-30. doi: 10.1002/ajmg.a.32902. Review.

PMID:
19681155
11.

KID syndrome (keratitis, ichthyosis, and deafness) and chronic mucocutaneous candidiasis: case report and review of the literature.

Harms M, Gilardi S, Levy PM, Saurat JH.

Pediatr Dermatol. 1984 Jul;2(1):1-7. Review.

PMID:
6390393
13.

"Curly" wood and tiger tails: an explanation for light and dark banding with polarization in trichothiodystrophy.

Sperling LC, DiGiovanna JJ.

Arch Dermatol. 2003 Sep;139(9):1189-92. Review.

PMID:
12975162
14.

[Collodion baby: 32 new case reports].

Larrègue M, Ottavy N, Bressieux JM, Lorette J.

Ann Dermatol Venereol. 1986;113(9):773-85. Review. French.

PMID:
3548541
15.

Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.

Itin PH, Sarasin A, Pittelkow MR.

J Am Acad Dermatol. 2001 Jun;44(6):891-920; quiz 921-4. Review.

PMID:
11369901
16.

Wiedemann-Rautenstrauch syndrome. A case report and review of the literature.

Stoll C, Labay F, Geisert J, Alembik Y.

Genet Couns. 1998;9(2):119-24. Review.

PMID:
9664208
17.

Skin manifestations of cardio-facio-cutaneous syndrome.

Borradori L, Blanchet-Bardon C.

J Am Acad Dermatol. 1993 May;28(5 Pt 2):815-9. Review.

PMID:
8491871
18.

Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: clinical and neuropathological observations in a 33-year-old man.

Keyvani K, Paulus W, Traupe H, Kiesewetter F, Cursiefen C, Huk W, Raab K, Orth U, Rauch A, Pfeiffer RA.

Am J Med Genet. 1998 Jul 24;78(4):371-7. Review.

PMID:
9714442
19.

Neu-Laxova syndrome: pathological evaluation of a fetus and review of the literature.

King JA, Gardner V, Chen H, Blackburn W.

Pediatr Pathol Lab Med. 1995 Jan-Feb;15(1):57-79. Review.

PMID:
8736598
20.

[Neurocutaneous syndrome with hair alterations].

Camacho-Martínez F.

Rev Neurol. 1997 Sep;25 Suppl 3:S243-9. Review. Spanish.

PMID:
9273169
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