Search research articles
Contact Us
Filters
Showing results (261-270 of 444) with videos related to
Page
of 45
Sort By:
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 26, 2018
Teledermatology-driven topical therapy of actinic keratosis: a comparative study of clinical effectiveness and compliance
L Ferrándiz, M Morales-Conde, A Fernández-Orland, et al.
Medicina Clinica
|
November 13, 2004
[Haplotype of the BRCA2 6857delAA mutation in 4 families with breast/ovarian cancer]
Berta Campos, Orland Díez, Carolina Alvarez, et al.
Frontiers in Neurology
|
June 21, 2024
Risk of epilepsy after traumatic brain injury: a nationwide Norwegian matched cohort study
Hild Flatmark Sødal, Trond Nordseth, Anders Johan Orland Rasmussen, et al.
Extremophiles : Life Under Extreme Conditions
|
February 19, 2008
Metabolism of halophilic archaea
Michaela Falb, Kerstin Müller, Lisa Königsmaier, et al.
The Journal of Heredity
|
May 14, 2022
A Draft Reference Genome Assembly of the Critically Endangered Black Abalone, Haliotis cracherodii
Chloé Orland, Merly Escalona, Ruta Sahasrabudhe, et al.
International Journal of Surgical Pathology
|
February 21, 2023
Difficult to Diagnose Cutaneous Melanoma in a Patient with BAP1 Tumor Predisposition Syndrome
Francisca Silva-Clavería, Alejandro Álvarez-Muñoz, Lara Ferrándiz, et al.
Journal of Surgical Orthopaedic Advances
|
March 11, 2026
Virtual Reality Improves Confidence and Short-Term Retention During Tibial Intramedullary Nail Insertion: A Randomized Trial
Mark D Orland, Matt Siegel, Lucas Paladino, et al.
Managed Care (Langhorne, Pa.)
|
December 4, 2001
Antiplatelet pathways development. Panel discussion
J Ballenger, J W Olin, L M Brass, et al.
Heart Rhythm
|
February 25, 2014
KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmia
Matthew M Kalscheur, Ravi Vaidyanathan, Kate M Orland, et al.
Medicina Clinica
|
October 31, 2002
[Description of a new TP53 gene germline mutation in a family with the Li-Fraumeni syndrome. Genetic counselling to healthy mutation carriers]
Judith Balmaña, Josep Nomdedéu, Orland Díez, et al.
Page
of 45
Search research articles
Search
Showing results (261-270 of 444) with videos related to
Sort By:
Page
of 45
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 26, 2018
Teledermatology-driven topical therapy of actinic keratosis: a comparative study of clinical effectiveness and compliance
L Ferrándiz, M Morales-Conde, A Fernández-Orland, et al.
Medicina Clinica
|
November 13, 2004
[Haplotype of the BRCA2 6857delAA mutation in 4 families with breast/ovarian cancer]
Berta Campos, Orland Díez, Carolina Alvarez, et al.
Frontiers in Neurology
|
June 21, 2024
Risk of epilepsy after traumatic brain injury: a nationwide Norwegian matched cohort study
Hild Flatmark Sødal, Trond Nordseth, Anders Johan Orland Rasmussen, et al.
Extremophiles : Life Under Extreme Conditions
|
February 19, 2008
Metabolism of halophilic archaea
Michaela Falb, Kerstin Müller, Lisa Königsmaier, et al.
The Journal of Heredity
|
May 14, 2022
A Draft Reference Genome Assembly of the Critically Endangered Black Abalone, Haliotis cracherodii
Chloé Orland, Merly Escalona, Ruta Sahasrabudhe, et al.
International Journal of Surgical Pathology
|
February 21, 2023
Difficult to Diagnose Cutaneous Melanoma in a Patient with BAP1 Tumor Predisposition Syndrome
Francisca Silva-Clavería, Alejandro Álvarez-Muñoz, Lara Ferrándiz, et al.
Journal of Surgical Orthopaedic Advances
|
March 11, 2026
Virtual Reality Improves Confidence and Short-Term Retention During Tibial Intramedullary Nail Insertion: A Randomized Trial
Mark D Orland, Matt Siegel, Lucas Paladino, et al.
Managed Care (Langhorne, Pa.)
|
December 4, 2001
Antiplatelet pathways development. Panel discussion
J Ballenger, J W Olin, L M Brass, et al.
Heart Rhythm
|
February 25, 2014
KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmia
Matthew M Kalscheur, Ravi Vaidyanathan, Kate M Orland, et al.
Medicina Clinica
|
October 31, 2002
[Description of a new TP53 gene germline mutation in a family with the Li-Fraumeni syndrome. Genetic counselling to healthy mutation carriers]
Judith Balmaña, Josep Nomdedéu, Orland Díez, et al.
Page
of 45