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Images of Flemming Wibrand
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Wyniki wyszukiwania
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Line Borgwardt, Christine I. Dali, Jens Fogh, Jan-Erik Mansson, Klaus J. Olsen, Hans C. Beck, Kim G. Nielsen, Lene Huche Nielsen, Svein Ottar E. Olsen, Hilde Monica Frostad Riise Stensland, Odd Nilssen, Flemming Wibrand, Anne Marie Thuesen, Taylor Pearl, Ulla Haugsted, Paul Saftig, Judith Blanz, Simon A. Jones, ...
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Flemming Wibrand Herlev Nuwber
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Navn: Flemming WibrandBy: Herlev, Postnummer: og mere information
Henning Haahr Andersen | AceMap
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http://linkinghub.elsevier.com/retrieve/pii/S · Neuromuscular Disorders - Tina Dysgaard Jeppesen, Morten Duno, Lotte Risom, Flemming Wibrand, Jabin Rafiq, Thomas O Krag, Johannes Jakobsen, Henning Haahr Andersen Chapter 29 Mechanisms of Disease Role of Neurotrophins in Diabetes ...
Interests
Discovery of CLPB gene associated with a new pediatric mitochondrial...
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A new study describes a new pediatric mitochondrial syndrome and discovery of the responsible gene, called CLPB. Researchers report findings based on gene...
Table of contents | Journal of Medical Genetics
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See the March 2015, Volume 52, Number 3 table of contents and sign up to receive a TOC email alert. Search this site Flemming Wibrand, Eric A Shoubridge,
CLPB Variants Associated with Autosomal-Recessive ...
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Flemming Wibrand. Search for articles by this author Affiliations. Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen ...
Mutations in COA3 cause isolated complex IV deficiency associated...
jmg.bmj.com
Lars Jønson,5 Morten Duno,1 Flemming Wibrand,1 Eric A Shoubridge,2 John Vissing6 1Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet
Business Profiles
Researchgate: Flemming Wibrand
Copenhagen, Denmark
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Books & Literature
JoVE | Peer Reviewed Scientific Video Journal - Methods and Protocols
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JoVE publishes peer-reviewed scientific video protocols to accelerate biological, medical, chemical and physical research. Watch our scientific video articles.
Taurine 6 - Google Books
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Svend Høime Hansen,1 Mogens Larsen Andersen, Henrik Birkedal, Claus Cornett, and Flemming Wibrand 1. ABSTRACT Several studies have demonstrated that especially high taurine concentrations are found in tissues with high oxidative activity, whereas lower concentrations are found in tissues with primary glycolytic ...
Plasma hypoxanthine reacts more abruptly to changes in oxygenation...
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Elisabeth Frøyland, Flemming Wibrand, Runar Almaas, Ingvild Dalen, Julie K Lindstad, and Terje Rootwelt. Pediatric Research, 2005, Volume 57, Number 4, Page DOI: PDR E. [3]. Effect of Barbiturates on Hydroxyl Radicals, Lipid Peroxidation, and Hypoxic Cell Death in Human NT2-N ...
JIMD Reports, Volume Reader - PaperC
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Sabine Grønborg, Niklas Darin, Maria J. Miranda, Bodil Damgaard, Jorge Asin Cayuela, Anders Oldfors, Gittan Kollberg, Thomas V. O. Hansen, Kirstine Ravn, Flemming Wibrand and Elsebet Østergaard. Peak Jump Power Reflects the Degree of Ambulatory Ability in Patients with Mitochondrial and Other ...
Related Documents
A novel de novo mutation of the mitochondrial...
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Flemming Wibrand. Search for articles by this author Affiliations. Department of Clinical Genetics, Rigshospitalet, University of Copenhagen, Denmark;
Table of contents, Muscle and Nerve | mus | DeepDyve
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Read "Table of contents" on ... PhD Limited Diagnostic Value of Enzyme Analysis in Patients With Mitochondrial tRNA Mutations Flemming Wibrand, PhD, Tina D ...
Late onset of stroke-like episode associated with a 3256C→T point ...
www.jns-journal.com
Department of Radiology, National University Hospital, Rigshospitalet, Copenhagen, Denmark. ,. Flemming Wibrand. x. Flemming Wibrand. Search for articles ...
31P-MRS of skeletal muscle is not a sensitive diagnostic test for...
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Bjørn Quistorff. Flemming Wibrand. John Vissing P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy.
Scientific Publications
Pure exercise intolerance and ophthalmoplegia associated with the...
bmcmusculoskeletdisord.biomedcentral.com
Pure exercise intolerance and ophthalmoplegia associated with the m.12,294G > A mutation in the MT-TL2 gene: a case report. Patrick SoldathEmail authorView ORCID ID profile,; Karen Lindhardt Madsen,; Astrid Emilie Buch,; Morten Duno,; Flemming Wibrand and; John Vissing. BMC Musculoskeletal DisordersBMC ...
Publications
Publications Authored by Flemming Wibrand | PubFacts.com
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Are you Flemming Wibrand? Claim your profile, edit publications, add additional information:
Exercise Intolerance and Myoglobinuria Associated with a Novel...
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The most common clinical phenotype caused by a mtDNA mutation in complex I of the mitochondrial respiratory chain is Leber hereditary optic neuropathy. We...
Details and Download Full Text PDF: A Patient with Complex I...
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Jessica Nouws, Flemming Wibrand, Mariël van den Brand, Hanka Venselaar, Morten Duno, Allan M Lund, Simon Trautner, Leo Nijtmans, Elsebet Ostergard. Download Full Paper.
31P-MRS of skeletal muscle is not a sensitive diagnostic test for...
link.springer.com
Bjørn Quistorff. NMR Center, The Panum InstituteUniversity of Copenhagen. Flemming Wibrand,. Flemming Wibrand. John F. Kennedy Institute. John Vissing ...
Miscellaneous
Flemming Wibrand - Publikationer - Forskning - Region Hovedstaden
research.regionh.dk
Flemming Wibrand. Klinisk Genetisk Afdeling , Juliane Marie Centret Rigshospitalet; Oversigt; Publikationer Tidsskrifter ud af 21 Pr. side: ; 25; 50;
Wibrand - Names Encyclopedia
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Flemming Wibrand (1) Bjarne Wibrand (1) Erik Wibrand (1) Jeanette Wibrand (1) Jesper Wibrand (1) Merete Wibrand (1) Morten Wibrand (1) Marianne Wibrand (1) Magnus ...
Flemming Wibrand - Forskning - Region Hovedstaden
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Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation. Publikation: Forskning - peer review › Tidsskriftartikel
Flemming Wibrand - Forskning - Rigshospitalet
research.regionh.dk
A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood. Publikation: Forskning ...
Flemming Wibrand - Tidsskrifter - Forskning - Region Hovedstaden
research.regionh.dk
Journal of Medical Genetics. ISSNs: B M J Group, Storbritannien. Central database. Tidsskrift
A mitochondrial tRNAMet mutation causing...
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Flemming Wibrand. x. Flemming Wibrand. Search for articles by this author Affiliations. Department of Clinical Genetics, University of Copenhagen, Rigshospitalet
Aerobic training is safe and improves exercise capacity in patients...
academic.oup.com
Tina D. Jeppesen 1, Marianne Schwartz 2, David B. Olsen 1, Flemming Wibrand 2, Thomas Krag 1, Morten Dunø 2, Simon Hauerslev 1 and ; John Vissing 1; 1 Department of
Biomarkers of mitochondrial content in skeletal muscle of healthy...
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Sigma-Aldrich offers abstracts and full-text articles by [Steen Larsen, Joachim Nielsen, Christina Neigaard Hansen, Lars Bo Nielsen, Flemming Wibrand, Nis...
15th Taurine Meeting
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16: :00, Svend Hoime Hansen, Henrik Birkedal, Mogens Larsen Andersen , Claus Cornett, and Flemming Wibrand (Copenhagen, Denmark): The important role of taurine in oxidative metabolism. 17: :30, Taesun Park, Haemi Lee, Sung-Hee Park, Kun-Koo Park, and Ha Won Kim (Seoul and Chunchon, Korea): ...
EBSCOhost | | 31P-MRS of skeletal muscle is not a sensitive...
web.b.ebscohost.com
Flemming Wibrand. John Vissing P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy. Received: 28 December Received in revised form: 8 March Accepted: 15 March Published online: 4 February □ Abstract Clinical phenotypes of persons with mitochondrial ...
Enzyme replacement therapy for alpha-mannosidosis - Syddansk...
findresearcher.sdu.dk
... HM and O Nilssen and Flemming Wibrand and AM Thuesen and T Pearl and U Haugsted and Paul Saftig and Judith Blanz and SA Jones and A Tylki-Szymanska and N
Alpha Mannosidosis
www.diseaseinfosearch.org
Author(s): Line Borgwardt, Hilde Monica Frostad Riise Stensland, Klaus Juul Olsen, Flemming Wibrand, Helle Bagterp Klenow, Michael Beck, Yasmina Amraoui, Laila Arash, Jens Fogh, Øivind Nilssen, Christine I Dali, Allan Meldgaard Lund. Journal: Alpha-mannosidosis is caused by mutations in MAN2B1, leading to loss of ...
A novel de novo mutation of the mitochondrial tRNA(lys) gene...
pure.au.dk
author = "Jeppesen, {Tina Dysgaard} and Morten Duno and Lotte Risom and Flemming Wibrand and Jabin Rafiq and Thomas Krag and Johannes Jakobsen ...
A novel mitochondrial mutation m.8989G>C associated with neuropathy,...
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VBN is the research portal for Aalborg University and presents research and research activities of AAU.
Table of Contents — May 14, 2013, 80 (20) | Neurology
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Flemming Wibrand, and John Vissing; May 14, : doi: ... Shao-Hua Yu, Chian-Ze Peng, Kuo-Wei Cheng, and Chorng-Kuang How; May 14, ...
Hearing impairment and renal failure associated with...
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Biomarkers of mitochondrial content in skeletal muscle of healthy...
research.ku.dk
author = "Steen Larsen and Joachim Nielsen and {Neigaard Nielsen}, Christina and Nielsen, {Lars Bo} and Flemming Wibrand and Nis Stride and Schroder, ...
CLPB variants associated with autosomal-recessive mitochondrial...
uncch.pure.elsevier.com
Carol Saunders ; Laurie Smith ; Flemming Wibrand ; Kirstine Ravn ; Peter Bross ; Isabelle Thiffault ; Mette Christensen ; Andrea Atherton ; Emily ...
Kompleks defekter (I-V) | Mitokondrieforeningen i Danmark
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Forfatter, John Vissing (overlæge) Flemming Skovby (professor, dr. med) Thomas Rosenberg (overlæge) Flemming Wibrand (biokemiker) Elsebet Østergaard ( læge) Nina Horn (biokemiker/afd.leder) (Tak til ovennævnte, der har alle bidraget til denne beskrivelse). Andre med samme diagnose? Der findes en forening for ...
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