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F Hoffmann

Showing results (891-900 of 1,255) with videos related to

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Arthritis and Rheumatism|November 1, 2008
Vertebral strength changes in rheumatoid arthritis patients treated with alendronate, as assessed by finite element analysis of clinical computed tomography scans: a prospective randomized clinical trialTaro Mawatari, Hiromasa Miura, Satoshi Hamai, et al.
Endocrine|November 8, 2023
Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project)Sebastian Gippert, Matias Wagner, Theresa Brunet, et al.
The Journal of Biological Chemistry|September 16, 2003
Methylmalonic acid, a biochemical hallmark of methylmalonic acidurias but no inhibitor of mitochondrial respiratory chainStefan Kölker, Marina Schwab, Friederike Hörster, et al.
Patient Education and Counseling|February 11, 2010
Outcome of parent-physician communication skills training for pediatric residentsChristoph Nikendei, Hans Martin Bosse, Katja Hoffmann, et al.
Bone Marrow Transplantation|June 6, 2017
MRD response in a refractory paediatric T-ALL patient through anti-programmed cell death 1 (PD-1) Ab treatment associated with induction of fatal GvHDA-M Boekstegers, F Blaeschke, I Schmid, et al.
Annals of Neurology|January 31, 2003
Lack of creatine in muscle and brain in an adult with GAMT deficiencyAndreas Schulze, Peter Bachert, Heinz Schlemmer, et al.
Annals of Human Genetics|April 3, 2001
A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorderR J Janssen, R A Wevers, M Häussler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1991
Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detectionG F Hoffmann, L Sweetman, H J Bremer, et al.
World Journal of Pediatrics : WJP|January 20, 2017
Newborn screening for remethylation disorders and vitamin B<sub>12</sub> deficiency-evaluation of new strategies in cohorts from Qatar and GermanyGwendolyn Gramer, Ghassan Abdoh, Tawfeg Ben-Omran, et al.
Metabolites|October 22, 2021
Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This ObservationDorothea Haas, Jana Hauke, Kathrin V Schwarz, et al.
Pageof 126

Showing results (891-900 of 1,255) with videos related to

Sort By:
Pageof 126
Arthritis and Rheumatism|November 1, 2008
Vertebral strength changes in rheumatoid arthritis patients treated with alendronate, as assessed by finite element analysis of clinical computed tomography scans: a prospective randomized clinical trialTaro Mawatari, Hiromasa Miura, Satoshi Hamai, et al.
Endocrine|November 8, 2023
Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project)Sebastian Gippert, Matias Wagner, Theresa Brunet, et al.
The Journal of Biological Chemistry|September 16, 2003
Methylmalonic acid, a biochemical hallmark of methylmalonic acidurias but no inhibitor of mitochondrial respiratory chainStefan Kölker, Marina Schwab, Friederike Hörster, et al.
Patient Education and Counseling|February 11, 2010
Outcome of parent-physician communication skills training for pediatric residentsChristoph Nikendei, Hans Martin Bosse, Katja Hoffmann, et al.
Bone Marrow Transplantation|June 6, 2017
MRD response in a refractory paediatric T-ALL patient through anti-programmed cell death 1 (PD-1) Ab treatment associated with induction of fatal GvHDA-M Boekstegers, F Blaeschke, I Schmid, et al.
Annals of Neurology|January 31, 2003
Lack of creatine in muscle and brain in an adult with GAMT deficiencyAndreas Schulze, Peter Bachert, Heinz Schlemmer, et al.
Annals of Human Genetics|April 3, 2001
A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorderR J Janssen, R A Wevers, M Häussler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1991
Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detectionG F Hoffmann, L Sweetman, H J Bremer, et al.
World Journal of Pediatrics : WJP|January 20, 2017
Newborn screening for remethylation disorders and vitamin B<sub>12</sub> deficiency-evaluation of new strategies in cohorts from Qatar and GermanyGwendolyn Gramer, Ghassan Abdoh, Tawfeg Ben-Omran, et al.
Metabolites|October 22, 2021
Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This ObservationDorothea Haas, Jana Hauke, Kathrin V Schwarz, et al.
Pageof 126