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Annales De Dermatologie Et De Venereologie
|
January 1, 1995
[Cutaneous transformation of chronic lymphoid leukemia into immunoblastic lymphoma. Cutaneous manifestation of Richter syndrome]
S Fraitag, C Bodemer, P Rousselot, et al.
The Journal of Pediatrics
|
December 1, 1994
Partial albinism with immunodeficiency (Griscelli syndrome)
C Klein, N Philippe, F Le Deist, et al.
The British Journal of Dermatology
|
July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases
C Bodemer, Y De Prost, B Bachollet, et al.
Dermatology (Basel, Switzerland)
|
June 19, 2010
Two congenital cases of pigmented epithelioid melanocytoma studied by fluorescent in situ hybridization for melanocytic tumors: case reports and review of these recent topics
M Battistella, M Prochazkova-Carlotti, D Berrebi, et al.
The British Journal of Dermatology
|
March 11, 2014
Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations
S Duchatelet, L Guibbal, S de Veer, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1986
[Gliomas of the uterus. Apropos of 3 cases and review of the literature]
R Kalifat, H Baup, S Fraitag, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
January 16, 2022
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation
S Leclerc-Mercier, S Mercier, N Bellon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 1, 1996
[Dermatitis herpetiformis occuring in patients with celiac disease in childhood]
N Démoulins-Giacco, V Gagey, D Teillac-Hamel, et al.
Clinical Genetics
|
April 24, 2010
Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form
E Sbidian, D Feldmann, J Bengoa, et al.
The British Journal of Dermatology
|
April 26, 2017
Skin manifestations among GATA2-deficient patients
A Polat, M Dinulescu, S Fraitag, et al.
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of 16
Search research articles
Search
Showing results (91-100 of 152) with videos related to
Sort By:
Page
of 16
Annales De Dermatologie Et De Venereologie
|
January 1, 1995
[Cutaneous transformation of chronic lymphoid leukemia into immunoblastic lymphoma. Cutaneous manifestation of Richter syndrome]
S Fraitag, C Bodemer, P Rousselot, et al.
The Journal of Pediatrics
|
December 1, 1994
Partial albinism with immunodeficiency (Griscelli syndrome)
C Klein, N Philippe, F Le Deist, et al.
The British Journal of Dermatology
|
July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases
C Bodemer, Y De Prost, B Bachollet, et al.
Dermatology (Basel, Switzerland)
|
June 19, 2010
Two congenital cases of pigmented epithelioid melanocytoma studied by fluorescent in situ hybridization for melanocytic tumors: case reports and review of these recent topics
M Battistella, M Prochazkova-Carlotti, D Berrebi, et al.
The British Journal of Dermatology
|
March 11, 2014
Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations
S Duchatelet, L Guibbal, S de Veer, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1986
[Gliomas of the uterus. Apropos of 3 cases and review of the literature]
R Kalifat, H Baup, S Fraitag, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
January 16, 2022
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation
S Leclerc-Mercier, S Mercier, N Bellon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 1, 1996
[Dermatitis herpetiformis occuring in patients with celiac disease in childhood]
N Démoulins-Giacco, V Gagey, D Teillac-Hamel, et al.
Clinical Genetics
|
April 24, 2010
Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form
E Sbidian, D Feldmann, J Bengoa, et al.
The British Journal of Dermatology
|
April 26, 2017
Skin manifestations among GATA2-deficient patients
A Polat, M Dinulescu, S Fraitag, et al.
Page
of 16