Hamel-Teillac D - Search Results

1

Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.

Chavanas S, Bodemer C, Rochat A, Hamel-Teillac D, Ali M, Irvine AD, Bonafé JL, Wilkinson J, Taïeb A, Barrandon Y, Harper JI, de Prost Y, Hovnanian A. Chavanas S, et al. Nat Genet. 2000 Jun;25(2):141-2. doi: 10.1038/75977. Nat Genet. 2000. PMID: 10835624

2

Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.

Bitoun E, Chavanas S, Irvine AD, Lonie L, Bodemer C, Paradisi M, Hamel-Teillac D, Ansai S, Mitsuhashi Y, Taïeb A, de Prost Y, Zambruno G, Harper JI, Hovnanian A. Bitoun E, et al. J Invest Dermatol. 2002 Feb;118(2):352-61. doi: 10.1046/j.1523-1747.2002.01603.x. J Invest Dermatol. 2002. PMID: 11841556 Free article.

3

An asymptomatic subcutaneous nodule of the lower back: a sentinel lesion for a diagnosis not to be missed.

Du-Thanh A, Hamel-Teillac D, De Prost Y, Bodemer C, Fraitag S. Du-Thanh A, et al. Am J Dermatopathol. 2013 Jul;35(5):595-6, 613-4. doi: 10.1097/DAD.0b013e3182863284. Am J Dermatopathol. 2013. PMID: 23449387 No abstract available.

4

[Febrile eruptions in systemic diseases in children].

Hamel-Teillac D, Bodemer C. Hamel-Teillac D, et al. Rev Prat. 1997 Sep 1;47(13):1458-62. Rev Prat. 1997. PMID: 9339027 French.

5

[Management of atopic dermatitis].

Hamel-Teillac D, de Prost Y. Hamel-Teillac D, et al. Rev Prat. 1998 May 1;48(9):979-81. Rev Prat. 1998. PMID: 11767357 Review. French.

6

[Localized scleroderma in children and a therapeutic trial using calcitriol: a therapeutic possibility to define].

Bodemer C, Amoric JC, Hamel-Teillac D, De Prost Y. Bodemer C, et al. Ann Dermatol Venereol. 1999 Oct;126(10):725-6. Ann Dermatol Venereol. 1999. PMID: 10604016 French. No abstract available.

7

[Rothmund-Thomson syndrome and defective DNA excision-resynthesis repair].

Bodak N, Bodemer C, Sarasin A, Hamel-Teillac D, Amoric JC, Pruszkowski A, De Prost Y. Bodak N, et al. Ann Dermatol Venereol. 2000 Jun-Jul;127(6-7):660-84. Ann Dermatol Venereol. 2000. PMID: 10930873 French. No abstract available.

8

Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations.

Hadj-Rabia S, Rimella A, Smahi A, Fraitag S, Hamel-Teillac D, Bonnefont JP, de Prost Y, Bodemer C. Hadj-Rabia S, et al. J Am Acad Dermatol. 2011 Mar;64(3):508-15. doi: 10.1016/j.jaad.2010.01.045. Epub 2011 Jan 20. J Am Acad Dermatol. 2011. PMID: 21255870

9

[Scleroderma in children: a retrospective study of 70 cases].

Bodemer C, Belon M, Hamel-Teillac D, Amoric JC, Fraitag S, Prieur AM, De Prost Y. Bodemer C, et al. Ann Dermatol Venereol. 1999 Oct;126(10):691-4. Ann Dermatol Venereol. 1999. PMID: 10604006 French.

10

[Hereditary cholestasis, an unusual etiology of pruritus in the infant].

Mahé E, Lacaille F, Hadj-Rabia S, Bodemer C, De Prost Y, Hamel-Teillac D. Mahé E, et al. Ann Dermatol Venereol. 2004 Dec;131(12):1092-4. doi: 10.1016/s0151-9638(04)93847-1. Ann Dermatol Venereol. 2004. PMID: 15692445 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

47 results

Search Page

Filters