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Molecular Syndromology
|
June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutation
P Brouillard, L M Boon, N Revencu, et al.
The British Journal of Dermatology
|
October 1, 2017
Clinical and haemodynamic risk factors associated with discrepancies in lower limb length with capillary malformations: data from the national paediatric French cohort CONAPE
M Samimi, M Durieux-Verde, A Caille, et al.
Journal of Medical Genetics
|
February 4, 2005
Mutational spectrum of NSDHL in CHILD syndrome
D Bornholdt, A König, R Happle, et al.
Oncogene
|
January 29, 2014
SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia
E Pasmant, B Gilbert-Dussardier, A Petit, et al.
Annales De Dermatologie Et De Venereologie
|
February 8, 2021
Acute acral eruptions in children during the COVID-19 pandemic: Characteristics of 103 children and their family clusters
T Hubiche, A Phan, S Leducq, et al.
The British Journal of Dermatology
|
January 23, 2016
Calculation of cut-off values based on the Autoimmune Bullous Skin Disorder Intensity Score (ABSIS) and Pemphigus Disease Area Index (PDAI) pemphigus scoring systems for defining moderate, significant and extensive types of pemphigus
C Boulard, S Duvert Lehembre, C Picard-Dahan, et al.
Annales De Dermatologie Et De Venereologie
|
March 13, 2016
[Impact of sex and age on the clinical and epidemiological aspects of childhood psoriasis: Data from a French cross-sectional multicentre study]
J Bonigen, A Phan, S Hadj-Rabia, et al.
Annales De Dermatologie Et De Venereologie
|
January 21, 2015
[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma]
M-F Avril, P Bahadoran, O Cabaret, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 13, 2021
Safety and efficacy of low-dose PI3K inhibitor taselisib in adult patients with CLOVES and Klippel-Trenaunay syndrome (KTS): the TOTEM trial, a phase 1/2 multicenter, open-label, single-arm study
M Luu, P Vabres, H Devilliers, et al.
Nature
|
June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium
A Smahi, G Courtois, P Vabres, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
Molecular Syndromology
|
June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutation
P Brouillard, L M Boon, N Revencu, et al.
The British Journal of Dermatology
|
October 1, 2017
Clinical and haemodynamic risk factors associated with discrepancies in lower limb length with capillary malformations: data from the national paediatric French cohort CONAPE
M Samimi, M Durieux-Verde, A Caille, et al.
Journal of Medical Genetics
|
February 4, 2005
Mutational spectrum of NSDHL in CHILD syndrome
D Bornholdt, A König, R Happle, et al.
Oncogene
|
January 29, 2014
SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia
E Pasmant, B Gilbert-Dussardier, A Petit, et al.
Annales De Dermatologie Et De Venereologie
|
February 8, 2021
Acute acral eruptions in children during the COVID-19 pandemic: Characteristics of 103 children and their family clusters
T Hubiche, A Phan, S Leducq, et al.
The British Journal of Dermatology
|
January 23, 2016
Calculation of cut-off values based on the Autoimmune Bullous Skin Disorder Intensity Score (ABSIS) and Pemphigus Disease Area Index (PDAI) pemphigus scoring systems for defining moderate, significant and extensive types of pemphigus
C Boulard, S Duvert Lehembre, C Picard-Dahan, et al.
Annales De Dermatologie Et De Venereologie
|
March 13, 2016
[Impact of sex and age on the clinical and epidemiological aspects of childhood psoriasis: Data from a French cross-sectional multicentre study]
J Bonigen, A Phan, S Hadj-Rabia, et al.
Annales De Dermatologie Et De Venereologie
|
January 21, 2015
[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma]
M-F Avril, P Bahadoran, O Cabaret, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 13, 2021
Safety and efficacy of low-dose PI3K inhibitor taselisib in adult patients with CLOVES and Klippel-Trenaunay syndrome (KTS): the TOTEM trial, a phase 1/2 multicenter, open-label, single-arm study
M Luu, P Vabres, H Devilliers, et al.
Nature
|
June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium
A Smahi, G Courtois, P Vabres, et al.
Page
of 9