Search research articles
Contact Us
Filters
Showing results (51-60 of 67) with videos related to
Page
of 7
Sort By:
Archives of Dermatology
|
June 19, 2001
Vesiculopustular eruptions in Down syndrome neonates with myeloproliferative disorders
A Nijhawan, E Baselga, M A Gonzalez-Ensenat, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 7, 2017
Infantile hemangiomas with minimal or arrested growth associated with soft tissue hypertrophy: a case series of 10 patients
S Planas-Ciudad, E Roé Crespo, I Sánchez-Carpintero, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2006
A prospective study of PHACE syndrome in infantile hemangiomas: demographic features, clinical findings, and complications
D W Metry, A N Haggstrom, B A Drolet, et al.
Molecular Syndromology
|
October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema
A Mendola, M J Schlögel, A Ghalamkarpour, et al.
Journal of Medical Genetics
|
February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect
P Brouillard, M Ghassibé, A Penington, et al.
The British Journal of Dermatology
|
May 22, 2015
Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership
A Hernández-Martín, P Dávila-Seijo, R de Lucas, et al.
Actas Dermo-Sifiliograficas
|
June 26, 2025
[Translated article] Update of the Spanish Consensus Document on Infantile Hemangioma
E Baselga, J Bernabeu-Wittel, I Betlloch Mas, et al.
Actas Dermo-Sifiliograficas
|
April 17, 2025
Update of the Spanish Consensus Document on Infantile Hemangioma
E Baselga, J Bernabeu-Wittel, I Betlloch Mas, et al.
Clinical and Experimental Dermatology
|
August 26, 2020
Capillary malformation-arteriovenous malformation syndrome: a multicentre study
M Valdivielso-Ramos, A Martin-Santiago, J M Azaña, et al.
The British Journal of Dermatology
|
January 30, 2019
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses
E Chacón-Solano, C León, F Díaz, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 67) with videos related to
Sort By:
Page
of 7
Archives of Dermatology
|
June 19, 2001
Vesiculopustular eruptions in Down syndrome neonates with myeloproliferative disorders
A Nijhawan, E Baselga, M A Gonzalez-Ensenat, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 7, 2017
Infantile hemangiomas with minimal or arrested growth associated with soft tissue hypertrophy: a case series of 10 patients
S Planas-Ciudad, E Roé Crespo, I Sánchez-Carpintero, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2006
A prospective study of PHACE syndrome in infantile hemangiomas: demographic features, clinical findings, and complications
D W Metry, A N Haggstrom, B A Drolet, et al.
Molecular Syndromology
|
October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema
A Mendola, M J Schlögel, A Ghalamkarpour, et al.
Journal of Medical Genetics
|
February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect
P Brouillard, M Ghassibé, A Penington, et al.
The British Journal of Dermatology
|
May 22, 2015
Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership
A Hernández-Martín, P Dávila-Seijo, R de Lucas, et al.
Actas Dermo-Sifiliograficas
|
June 26, 2025
[Translated article] Update of the Spanish Consensus Document on Infantile Hemangioma
E Baselga, J Bernabeu-Wittel, I Betlloch Mas, et al.
Actas Dermo-Sifiliograficas
|
April 17, 2025
Update of the Spanish Consensus Document on Infantile Hemangioma
E Baselga, J Bernabeu-Wittel, I Betlloch Mas, et al.
Clinical and Experimental Dermatology
|
August 26, 2020
Capillary malformation-arteriovenous malformation syndrome: a multicentre study
M Valdivielso-Ramos, A Martin-Santiago, J M Azaña, et al.
The British Journal of Dermatology
|
January 30, 2019
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses
E Chacón-Solano, C León, F Díaz, et al.
Page
of 7