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Isabel Colmenero

Showing results (81-90 of 112) with videos related to

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Pediatric Dermatology|September 8, 2015
Neonatal Lupus Erythematosus Mimicking Extensive Capillary MalformationFrancisco Vílchez-Márquez, Adriana Martín-Fuentes, Raquel Conejero, et al.
Pediatric Dermatology|April 15, 2021
Diffuse reticulate purpura in two adolescents with anorexia nervosa and severe malnutritionAna Mateos-Mayo, James Anderson-Vildósola, María Goretti Morón-Nozaleda, et al.
Pediatric Dermatology|September 1, 2018
Chronic urticaria in infants as the first manifestation of autoinflammatory diseaseIrene Latour, Lucero Noguera-Morel, Isabel Colmenero, et al.
Journal of Cutaneous Pathology|July 15, 2011
Dermatomyofibromas presenting in pediatric patients: clinicopathologic characteristics and differential diagnosisJuan C Tardío, Daniel Azorín, Almudena Hernández-Núñez, et al.
Journal of Cutaneous Pathology|August 11, 2017
Congenital cutaneous lymphadenomaAngel Fernandez-Flores, Ina Nicklaus-Wollenteit, Dharshini Sathishkumar, et al.
BMC Research Notes|June 29, 2016
Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case reportAsheeta Gupta, Isabel Colmenero, Nicola K Ragge, et al.
Journal of Cutaneous Pathology|January 24, 2023
Atrophic macules containing mesenchymal cells are precursor lesions of osteoma cutis in Albright hereditary osteodystrophyAntonio Torrelo, Laura Pericet, Isabel Hernández-Sürmann, et al.
Journal of Dermatological Science|November 6, 2009
The H syndrome: two novel mutations affecting the same amino acid residue of hENT3Vered Molho-Pessach, José Suarez, Christophe Perrin, et al.
The British Journal of Ophthalmology|February 13, 2019
Non-invasive diagnosis of retinoblastoma using cell-free DNA from aqueous humourAmy Gerrish, Edward Stone, Samuel Clokie, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
Pageof 12

Showing results (81-90 of 112) with videos related to

Sort By:
Pageof 12
Pediatric Dermatology|September 8, 2015
Neonatal Lupus Erythematosus Mimicking Extensive Capillary MalformationFrancisco Vílchez-Márquez, Adriana Martín-Fuentes, Raquel Conejero, et al.
Pediatric Dermatology|April 15, 2021
Diffuse reticulate purpura in two adolescents with anorexia nervosa and severe malnutritionAna Mateos-Mayo, James Anderson-Vildósola, María Goretti Morón-Nozaleda, et al.
Pediatric Dermatology|September 1, 2018
Chronic urticaria in infants as the first manifestation of autoinflammatory diseaseIrene Latour, Lucero Noguera-Morel, Isabel Colmenero, et al.
Journal of Cutaneous Pathology|July 15, 2011
Dermatomyofibromas presenting in pediatric patients: clinicopathologic characteristics and differential diagnosisJuan C Tardío, Daniel Azorín, Almudena Hernández-Núñez, et al.
Journal of Cutaneous Pathology|August 11, 2017
Congenital cutaneous lymphadenomaAngel Fernandez-Flores, Ina Nicklaus-Wollenteit, Dharshini Sathishkumar, et al.
BMC Research Notes|June 29, 2016
Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case reportAsheeta Gupta, Isabel Colmenero, Nicola K Ragge, et al.
Journal of Cutaneous Pathology|January 24, 2023
Atrophic macules containing mesenchymal cells are precursor lesions of osteoma cutis in Albright hereditary osteodystrophyAntonio Torrelo, Laura Pericet, Isabel Hernández-Sürmann, et al.
Journal of Dermatological Science|November 6, 2009
The H syndrome: two novel mutations affecting the same amino acid residue of hENT3Vered Molho-Pessach, José Suarez, Christophe Perrin, et al.
The British Journal of Ophthalmology|February 13, 2019
Non-invasive diagnosis of retinoblastoma using cell-free DNA from aqueous humourAmy Gerrish, Edward Stone, Samuel Clokie, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
Pageof 12