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David Adams

Showing results (251-260 of 370) with videos related to

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American Journal of Medical Genetics. Part A|November 14, 2008
Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiencyDespina Contopoulos-Ioannidis, Athanasios Evangeliou, Henk ter Laak, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|February 27, 2013
American Society of Echocardiography: Remote Echocardiography with Web-Based Assessments for Referrals at a Distance (ASE-REWARD) StudyShanemeet Singh, Manish Bansal, Puneet Maheshwari, et al.
American Journal of Human Genetics|May 6, 2017
Retraction Notice to: A BLOC-1 Mutation Screen Reveals that PLDN Is Mutated in Hermansky-Pudlak Syndrome Type 9Andrew R Cullinane, James A Curry, Carmelo Carmona-Rivera, et al.
Nature Communications|January 22, 2020
Mutational signatures in tumours induced by high and low energy radiation in Trp53 deficient miceYun Rose Li, Kyle D Halliwill, Cassandra J Adams, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 2, 2022
Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosisYukio Ando, David Adams, Merrill D Benson, et al.
Epilepsia|November 24, 2025
EEG functional connectivity as a marker of evolution from infantile epileptic spasms syndrome to Lennox-Gastaut syndromeBlanca Romero Milà, Virginia B Liu, Rachel J Smith, et al.
American Journal of Human Genetics|June 14, 2011
A BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak Syndrome type 9Andrew R Cullinane, James A Curry, Carmelo Carmona-Rivera, et al.
JACC. Cardiovascular Imaging|November 14, 2016
Cardiac Dysautonomia Predicts Long-Term Survival in Hereditary Transthyretin Amyloidosis After Liver TransplantationVincent Algalarrondo, Teresa Antonini, Marie Théaudin, et al.
Annals of Neurology|September 16, 2015
Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in FranceLouise-Laure Mariani, Pierre Lozeron, Marie Théaudin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2023
Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriersDiane Beauvais, Céline Labeyrie, Cécile Cauquil, et al.
Pageof 37

Showing results (251-260 of 370) with videos related to

Sort By:
Pageof 37
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiencyDespina Contopoulos-Ioannidis, Athanasios Evangeliou, Henk ter Laak, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|February 27, 2013
American Society of Echocardiography: Remote Echocardiography with Web-Based Assessments for Referrals at a Distance (ASE-REWARD) StudyShanemeet Singh, Manish Bansal, Puneet Maheshwari, et al.
American Journal of Human Genetics|May 6, 2017
Retraction Notice to: A BLOC-1 Mutation Screen Reveals that PLDN Is Mutated in Hermansky-Pudlak Syndrome Type 9Andrew R Cullinane, James A Curry, Carmelo Carmona-Rivera, et al.
Nature Communications|January 22, 2020
Mutational signatures in tumours induced by high and low energy radiation in Trp53 deficient miceYun Rose Li, Kyle D Halliwill, Cassandra J Adams, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 2, 2022
Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosisYukio Ando, David Adams, Merrill D Benson, et al.
Epilepsia|November 24, 2025
EEG functional connectivity as a marker of evolution from infantile epileptic spasms syndrome to Lennox-Gastaut syndromeBlanca Romero Milà, Virginia B Liu, Rachel J Smith, et al.
American Journal of Human Genetics|June 14, 2011
A BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak Syndrome type 9Andrew R Cullinane, James A Curry, Carmelo Carmona-Rivera, et al.
JACC. Cardiovascular Imaging|November 14, 2016
Cardiac Dysautonomia Predicts Long-Term Survival in Hereditary Transthyretin Amyloidosis After Liver TransplantationVincent Algalarrondo, Teresa Antonini, Marie Théaudin, et al.
Annals of Neurology|September 16, 2015
Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in FranceLouise-Laure Mariani, Pierre Lozeron, Marie Théaudin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2023
Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriersDiane Beauvais, Céline Labeyrie, Cécile Cauquil, et al.
Pageof 37