Fraitag S - Search Results

1

Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations.

Duchatelet S, Guibbal L, de Veer S, Fraitag S, Nitschké P, Zarhrate M, Bodemer C, Hovnanian A. Duchatelet S, et al. Among authors: fraitag s. Br J Dermatol. 2014 Sep;171(3):675-8. doi: 10.1111/bjd.12951. Epub 2014 Aug 4. Br J Dermatol. 2014. PMID: 24606194 No abstract available.

2

[Diagnosis of cutaneous nodules in the newborn and infant].

Fraitag S, Bodemer C. Fraitag S, et al. Ann Pathol. 1992;12(4-5):255-62. Ann Pathol. 1992. PMID: 1466681 French. No abstract available.

3

Immunohistochemical detection of granulocyte/macrophage colony-stimulating factor in Langerhans' cell histiocytosis.

Emile JF, Peuchmaur M, Fraitag S, Bodemer C, Brousse N. Emile JF, et al. Among authors: fraitag s. Histopathology. 1993 Oct;23(4):327-32. doi: 10.1111/j.1365-2559.1993.tb01215.x. Histopathology. 1993. PMID: 7507881

4

Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases.

Bodemer C, De Prost Y, Bachollet B, Poggi F, Teillac-Hamel D, Fraitag S, Saudubray JM. Bodemer C, et al. Among authors: fraitag s. Br J Dermatol. 1994 Jul;131(1):93-8. doi: 10.1111/j.1365-2133.1994.tb08463.x. Br J Dermatol. 1994. PMID: 8043426

5

Pityriasis lichenoides of childhood with atypical CD30-positive cells and clonal T-cell receptor gene rearrangements.

Panhans A, Bodemer C, Macinthyre E, Fraitag S, Paul C, de Prost Y. Panhans A, et al. Among authors: fraitag s. J Am Acad Dermatol. 1996 Sep;35(3 Pt 1):489-90. doi: 10.1016/s0190-9622(96)90639-8. J Am Acad Dermatol. 1996. PMID: 8784298 No abstract available.

6

Moderate and transient transfusion-associated cutaneous graft-versus-host disease in a child infected by human immunodeficiency virus.

Klein C, Fraitag S, Foulon E, Raffoux C, Bodemer C, Blanche S. Klein C, et al. Among authors: fraitag s. Am J Med. 1996 Oct;101(4):445-6. doi: 10.1016/s0002-9343(97)89433-8. Am J Med. 1996. PMID: 8873516 No abstract available.

7

Epidermolysis bullosa acquisita in childhood.

Callot-Mellot C, Bodemer C, Caux F, Bourgault-Villada I, Fraitag S, Goudié G, Heller M, de Prost Y, Prost C. Callot-Mellot C, et al. Among authors: fraitag s. Arch Dermatol. 1997 Sep;133(9):1122-6. Arch Dermatol. 1997. PMID: 9301589 Review.

8

Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation.

Hovnanian A, Rochat A, Bodemer C, Petit E, Rivers CA, Prost C, Fraitag S, Christiano AM, Uitto J, Lathrop M, Barrandon Y, de Prost Y. Hovnanian A, et al. Among authors: fraitag s. Am J Hum Genet. 1997 Sep;61(3):599-610. doi: 10.1086/515495. Am J Hum Genet. 1997. PMID: 9326325 Free PMC article.

9

Treatment of cutaneous lymphoid hyperplasia with thalidomide: report of two cases.

Benchikhi H, Bodemer C, Fraitag S, Wechsler J, Delfau-Larue MH, Gounod N, de Prost Y, Revuz J, Bagot M. Benchikhi H, et al. Among authors: fraitag s. J Am Acad Dermatol. 1999 Jun;40(6 Pt 1):1005-7. doi: 10.1016/s0190-9622(99)70094-0. J Am Acad Dermatol. 1999. PMID: 10365937

10

[Cutaneous nodules in neonates].

Bodemer C, Fraitag S. Bodemer C, et al. Among authors: fraitag s. Ann Dermatol Venereol. 1999 Dec;126(12):965-74. Ann Dermatol Venereol. 1999. PMID: 10648976 Review. French. No abstract available.

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