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Clinical and Experimental Dermatology
|
October 1, 2013
Ectodermal dysplasia-skin fragility syndrome: a novel mutation in the PKP1 gene
A Hernández-Martín, A Torrelo, S Ciria, et al.
Marine Environmental Research
|
July 26, 2024
Feeding strategies of the pelagic stingray (Pteroplatytrygon violacea) in the western Mediterranean Sea
Maria Vigo, Claudio Barría, Marta Nadal, et al.
Actas Dermo-Sifiliograficas
|
November 20, 2019
Spitz Nevus and Other Spitzoid Tumors in Children. Part 2: Cytogenetic and Molecular Features. Prognosis and Treatment
L Sainz-Gaspar, J Sánchez-Bernal, L Noguera-Morel, et al.
Actas Dermo-Sifiliograficas
|
December 3, 2019
Spitz Nevus and Other Spitzoid Tumors in Children -Part 1: Clinical, Histopathologic, and Immunohistochemical Features
L Sainz-Gaspar, J Sánchez-Bernal, L Noguera-Morel, et al.
The British Journal of Dermatology
|
May 24, 2019
Happle-Tinschert, Curry-Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum
M-L Lovgren, Y Zhou, G Hrčková, et al.
The British Journal of Dermatology
|
August 17, 2020
Chilblains and COVID-19: why SARS-CoV-2 endothelial infection is questioned. Reply from the authors
I Colmenero, C Santonja, M Alonso-Riaño, et al.
The British Journal of Dermatology
|
December 16, 2020
SARS-CoV-2 has not been detected directly by electron microscopy in the endothelium of chilblain lesions: reply from the authors
I Colmenero, C Santonja, M Alonso-Riaño, et al.
The British Journal of Dermatology
|
October 1, 2020
SARS-CoV-2 Has Not Been Detected Directly by Electron Microscopy in the Endothelium of Chilblain Lesions: reply from authors
I Colmenero, C Santonja, M Alonso-Riaño, et al.
The British Journal of Dermatology
|
June 11, 2013
Molecular evidence of type 2 mosaicism in Gorlin syndrome
A Torrelo, A Hernández-Martín, E Bueno, et al.
Cancer Genetics and Cytogenetics
|
December 31, 2002
Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma
M Urioste, A Martínez-Ramírez, J C Cigudosa, et al.
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of 7
Search research articles
Search
Showing results (31-40 of 65) with videos related to
Sort By:
Page
of 7
Clinical and Experimental Dermatology
|
October 1, 2013
Ectodermal dysplasia-skin fragility syndrome: a novel mutation in the PKP1 gene
A Hernández-Martín, A Torrelo, S Ciria, et al.
Marine Environmental Research
|
July 26, 2024
Feeding strategies of the pelagic stingray (Pteroplatytrygon violacea) in the western Mediterranean Sea
Maria Vigo, Claudio Barría, Marta Nadal, et al.
Actas Dermo-Sifiliograficas
|
November 20, 2019
Spitz Nevus and Other Spitzoid Tumors in Children. Part 2: Cytogenetic and Molecular Features. Prognosis and Treatment
L Sainz-Gaspar, J Sánchez-Bernal, L Noguera-Morel, et al.
Actas Dermo-Sifiliograficas
|
December 3, 2019
Spitz Nevus and Other Spitzoid Tumors in Children -Part 1: Clinical, Histopathologic, and Immunohistochemical Features
L Sainz-Gaspar, J Sánchez-Bernal, L Noguera-Morel, et al.
The British Journal of Dermatology
|
May 24, 2019
Happle-Tinschert, Curry-Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum
M-L Lovgren, Y Zhou, G Hrčková, et al.
The British Journal of Dermatology
|
August 17, 2020
Chilblains and COVID-19: why SARS-CoV-2 endothelial infection is questioned. Reply from the authors
I Colmenero, C Santonja, M Alonso-Riaño, et al.
The British Journal of Dermatology
|
December 16, 2020
SARS-CoV-2 has not been detected directly by electron microscopy in the endothelium of chilblain lesions: reply from the authors
I Colmenero, C Santonja, M Alonso-Riaño, et al.
The British Journal of Dermatology
|
October 1, 2020
SARS-CoV-2 Has Not Been Detected Directly by Electron Microscopy in the Endothelium of Chilblain Lesions: reply from authors
I Colmenero, C Santonja, M Alonso-Riaño, et al.
The British Journal of Dermatology
|
June 11, 2013
Molecular evidence of type 2 mosaicism in Gorlin syndrome
A Torrelo, A Hernández-Martín, E Bueno, et al.
Cancer Genetics and Cytogenetics
|
December 31, 2002
Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma
M Urioste, A Martínez-Ramírez, J C Cigudosa, et al.
Page
of 7