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Showing results (1021-1030 of 1,073) with videos related to
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Acta Psychiatrica Scandinavica
|
May 15, 2017
International trends in clozapine use: a study in 17 countries
C J Bachmann, L Aagaard, M Bernardo, et al.
Annals of Surgery
|
November 8, 2014
Multicenter double-blinded randomized controlled trial of standard abdominal wound edge protection with surgical dressings versus coverage with a sterile circular polyethylene drape for prevention of surgical site infections: a CHIR-Net trial (BaFO; NCT01181206)
André L Mihaljevic, Rebekka Schirren, Mine Özer, et al.
American Journal of Human Genetics
|
November 8, 2018
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy
Katharina Danhauser, Bader Alhaddad, Christine Makowski, et al.
Nature Genetics
|
December 11, 2012
Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy
Thomas Cullup, Ay Lin Kho, Carlo Dionisi-Vici, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2020
Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1
Dominic Lenz, Desirée E C Smith, Ellen Crushell, et al.
Brain : a Journal of Neurology
|
May 1, 2010
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis
Michèl A Willemsen, Marcel M Verbeek, Erik-Jan Kamsteeg, et al.
American Journal of Human Genetics
|
May 15, 2018
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy
Arcangela Iuso, Marit Wiersma, Hans-Joachim Schüller, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
July 7, 2025
Paediatric acute liver failure: A prospective, nationwide, population-based surveillance study in Germany
Dominic Lenz, Muhammad Abdulaziz, Bianca Peters, et al.
American Journal of Human Genetics
|
January 31, 2017
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
Yair Anikster, Tobias B Haack, Thierry Vilboux, et al.
Journal of Inherited Metabolic Disease
|
July 10, 2021
Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry
Mareike Keller, Heiko Brennenstuhl, Oya Kuseyri Hübschmann, et al.
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Search research articles
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Showing results (1021-1030 of 1,073) with videos related to
Sort By:
Page
of 108
Acta Psychiatrica Scandinavica
|
May 15, 2017
International trends in clozapine use: a study in 17 countries
C J Bachmann, L Aagaard, M Bernardo, et al.
Annals of Surgery
|
November 8, 2014
Multicenter double-blinded randomized controlled trial of standard abdominal wound edge protection with surgical dressings versus coverage with a sterile circular polyethylene drape for prevention of surgical site infections: a CHIR-Net trial (BaFO; NCT01181206)
André L Mihaljevic, Rebekka Schirren, Mine Özer, et al.
American Journal of Human Genetics
|
November 8, 2018
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy
Katharina Danhauser, Bader Alhaddad, Christine Makowski, et al.
Nature Genetics
|
December 11, 2012
Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy
Thomas Cullup, Ay Lin Kho, Carlo Dionisi-Vici, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2020
Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1
Dominic Lenz, Desirée E C Smith, Ellen Crushell, et al.
Brain : a Journal of Neurology
|
May 1, 2010
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis
Michèl A Willemsen, Marcel M Verbeek, Erik-Jan Kamsteeg, et al.
American Journal of Human Genetics
|
May 15, 2018
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy
Arcangela Iuso, Marit Wiersma, Hans-Joachim Schüller, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
July 7, 2025
Paediatric acute liver failure: A prospective, nationwide, population-based surveillance study in Germany
Dominic Lenz, Muhammad Abdulaziz, Bianca Peters, et al.
American Journal of Human Genetics
|
January 31, 2017
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
Yair Anikster, Tobias B Haack, Thierry Vilboux, et al.
Journal of Inherited Metabolic Disease
|
July 10, 2021
Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry
Mareike Keller, Heiko Brennenstuhl, Oya Kuseyri Hübschmann, et al.
Page
of 108