Search research articles
Contact Us
Filters
Showing results (471-480 of 544) with videos related to
Page
of 55
Sort By:
Human Mutation
|
July 19, 2008
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
W Edward Visser, Jurgen Jansen, Edith C H Friesema, et al.
Translational Oncology
|
June 24, 2020
Characteristics of head and neck squamous cell carcinoma cell Lines reflect human tumor biology independent of primary etiologies and HPV status
Thankam S Nair, Trey B Thomas, Lucy Yang, et al.
The American Journal of Clinical Nutrition
|
October 9, 2024
A cross-sectional study of associations between the <sup>13</sup>C-sucrose breath test, the lactulose rhamnose assay, and growth in children at high risk of environmental enteropathy
Nirupama Shivakumar, Sayeeda Huq, Maribel Paredes-Olortegui, et al.
Journal of Medical Genetics
|
May 1, 1992
Oculoauriculovertebral spectrum and cerebral anomalies
C T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, et al.
JACC. Clinical Electrophysiology
|
May 16, 2018
Acute and 3-Month Performance of a Communicating Leadless Antitachycardia Pacemaker and Subcutaneous Implantable Defibrillator
Fleur V Y Tjong, Tom F Brouwer, Brendan Koop, et al.
BMC Psychiatry
|
June 13, 2019
The decision tool unipolar depression (DTUD): a new measure to facilitate the early identification of patients with major depressive disorder in need of highly specialized care
Frédérique C W van Krugten, Maartje Goorden, Anton J L M van Balkom, et al.
Epilepsia
|
March 22, 2016
Neuronal antibodies in pediatric epilepsy: Clinical features and long-term outcomes of a historical cohort not treated with immunotherapy
Sukhvir Wright, Ada T Geerts, Cornelia Maria Jol-van der Zijde, et al.
Clinical Genetics
|
March 19, 2010
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum
J Van Reeuwijk, M J W Olderode-Berends, C Van den Elzen, et al.
Journal of Cardiovascular Electrophysiology
|
September 20, 2018
Feasibility of subcutaneous implantable cardioverter-defibrillator implantation with opioid sparing truncal plane blocks and deep sedation
Marc A Miller, Jalaj Garg, Benjamin Salter, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 2, 2015
Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment
Martje E van Egmond, Jan Willem J Elting, Anouk Kuiper, et al.
Page
of 55
Search research articles
Search
Showing results (471-480 of 544) with videos related to
Sort By:
Page
of 55
Human Mutation
|
July 19, 2008
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
W Edward Visser, Jurgen Jansen, Edith C H Friesema, et al.
Translational Oncology
|
June 24, 2020
Characteristics of head and neck squamous cell carcinoma cell Lines reflect human tumor biology independent of primary etiologies and HPV status
Thankam S Nair, Trey B Thomas, Lucy Yang, et al.
The American Journal of Clinical Nutrition
|
October 9, 2024
A cross-sectional study of associations between the <sup>13</sup>C-sucrose breath test, the lactulose rhamnose assay, and growth in children at high risk of environmental enteropathy
Nirupama Shivakumar, Sayeeda Huq, Maribel Paredes-Olortegui, et al.
Journal of Medical Genetics
|
May 1, 1992
Oculoauriculovertebral spectrum and cerebral anomalies
C T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, et al.
JACC. Clinical Electrophysiology
|
May 16, 2018
Acute and 3-Month Performance of a Communicating Leadless Antitachycardia Pacemaker and Subcutaneous Implantable Defibrillator
Fleur V Y Tjong, Tom F Brouwer, Brendan Koop, et al.
BMC Psychiatry
|
June 13, 2019
The decision tool unipolar depression (DTUD): a new measure to facilitate the early identification of patients with major depressive disorder in need of highly specialized care
Frédérique C W van Krugten, Maartje Goorden, Anton J L M van Balkom, et al.
Epilepsia
|
March 22, 2016
Neuronal antibodies in pediatric epilepsy: Clinical features and long-term outcomes of a historical cohort not treated with immunotherapy
Sukhvir Wright, Ada T Geerts, Cornelia Maria Jol-van der Zijde, et al.
Clinical Genetics
|
March 19, 2010
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum
J Van Reeuwijk, M J W Olderode-Berends, C Van den Elzen, et al.
Journal of Cardiovascular Electrophysiology
|
September 20, 2018
Feasibility of subcutaneous implantable cardioverter-defibrillator implantation with opioid sparing truncal plane blocks and deep sedation
Marc A Miller, Jalaj Garg, Benjamin Salter, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 2, 2015
Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment
Martje E van Egmond, Jan Willem J Elting, Anouk Kuiper, et al.
Page
of 55