Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marietta Clewing"'
Publikováno v:
Methodist Debakey Cardiovasc J
Loperamide, a μ-opioid receptor agonist, can cause cardiotoxicity by inhibiting the potassium ion channel and slowing cardiomyocyte repolarization. This, in turn, can lead to frequent early afterdepolarizations, the most common mechanism of drug-ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4caf69596a19ffc40d60092351339d5
https://europepmc.org/articles/PMC8158447/
https://europepmc.org/articles/PMC8158447/
Autor:
Aryan Nezamabadi, Richard J. Robbins, Johanna Marietta Clewing, Richard Ogunti, Jose A. Perez, Lara Colton, Sayali Ketkar, Mamta Puppala, Stephen T. C. Wong, Melina Awar
Publikováno v:
Academic Medicine. 93:491-497
To compare costs of care and quality outcomes between teaching and nonteaching hospitalist services, while testing the assumption that resident-driven care is more expensive.Records of inpatients with the top 20 Medicare Severity Diagnosis-Related Gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac9e802c672f0d5ea680babe80271072
https://doi.org/10.1097/acm.0000000000002026
https://doi.org/10.1097/acm.0000000000002026
Publikováno v:
The American journal of medicine. 132(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8713702edad5641b4af60c884a9b76f9
https://pubmed.ncbi.nlm.nih.gov/29864414
https://pubmed.ncbi.nlm.nih.gov/29864414
Autor:
Michael Knauth, Cornelius F. Boerkoel, Anibh M. Das, Johanna Marietta Clewing, Hans Hartmann, Thomas Lücke, Frank Donnerstag, Hartmut Becker
Publikováno v:
American Journal of Medical Genetics Part A. :2040-2045
Schimke-immuno-osseous dysplasia is an autosomal-recessive multisystem disorder with the prominent clinical features disproportionate growth failure, progressive renal failure, and T-cell immunodeficiency. Neurological symptoms caused by transient is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1c47f95c613ba964a643451134f4d48
https://doi.org/10.1002/ajmg.a.31878
https://doi.org/10.1002/ajmg.a.31878
Publikováno v:
The Journal of surgical research. 185(2)
Background Anorectal manometry is used extensively in the assessment of patients with disorders of the pelvic floor. The present study investigated the repeatability of anorectal manometry in healthy volunteers and patients. Patients and methods A to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8966fea1a9e46a8e3a360b1692b34163
https://pubmed.ncbi.nlm.nih.gov/23968807
https://pubmed.ncbi.nlm.nih.gov/23968807
Autor:
François Nobili, Lawrence R. Shoemaker, David V. Milford, Mitra Basiratnia, Anna Buck, Georges Deschênes, Isabel Cordeiro, Jorge M. Saraiva, Helen Fryssira, Anja Stein, Behzad Najafian, Natasa Stajic, Laura Massella, Joel Charrow, Glenda Hendson, Umakumaran Ponniah, Thomas Lücke, M. Semin Fenkçi, Doris Taha, Elena Levtchenko, J. Marietta Clewing, Pierre Frange, Yumi Asakura, Christine Kobelka, Jean Luc André, David M. Parham, Jonathan Zonana, Radovan Bogdanovic, Justin Weinkauf, Zhongxin Yu, C. Nur Semerci, Stefan Fründ, Arend Bökenkamp, Cornelius F. Boerkoel, Salman Kirmani, Dorothea Wand, Peter Stenzel, Kory Keller, David B. Lewis, Pierre Cochat, Marie Morimoto, Christy Mayfield, Encarna Guillén-Navarro, D. Ross McLeod, Andrew K. Gormley, Petra Lamfers, Dominique Bonneau
Publikováno v:
Orphanet Journal of Rare Diseases, 7:70. BioMed Central
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 70 (2012)
Morimoto, M, Yu, Z X, Stenzel, P, Clewing, J M, Najafian, B, Mayfield, C, Hendson, G, Weinkauf, J G, Gormley, A K, Parham, D M, Ponniah, U, Andre, J L, Asakura, Y, Basiratnia, M, Bogdanovic, R, Bokenkamp, A, Bonneau, D, Buck, A, Charrow, J, Cochat, P, Cordeiro, I, Deschenes, G, Fenkci, M S, Frange, P, Frund, S, Fryssira, H, Guillen-Navarro, E, Keller, K, Kirmani, S, Kobelka, C, Lamfers, P, Levtchenko, E, Lewis, D B, Massella, L, Mcleod, D R, Milford, D V, Nobili, F, Saraiva, J M, Semerci, C N, Shoemaker, L, Stajic, N, Stein, A, Taha, D, Wand, D, Zonana, J, Lucke, T & Boerkoel, C F 2012, ' Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia? ', Orphanet Journal of Rare Diseases, vol. 7, 70 . https://doi.org/10.1186/1750-1172-7-70
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 70 (2012)
Morimoto, M, Yu, Z X, Stenzel, P, Clewing, J M, Najafian, B, Mayfield, C, Hendson, G, Weinkauf, J G, Gormley, A K, Parham, D M, Ponniah, U, Andre, J L, Asakura, Y, Basiratnia, M, Bogdanovic, R, Bokenkamp, A, Bonneau, D, Buck, A, Charrow, J, Cochat, P, Cordeiro, I, Deschenes, G, Fenkci, M S, Frange, P, Frund, S, Fryssira, H, Guillen-Navarro, E, Keller, K, Kirmani, S, Kobelka, C, Lamfers, P, Levtchenko, E, Lewis, D B, Massella, L, Mcleod, D R, Milford, D V, Nobili, F, Saraiva, J M, Semerci, C N, Shoemaker, L, Stajic, N, Stein, A, Taha, D, Wand, D, Zonana, J, Lucke, T & Boerkoel, C F 2012, ' Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia? ', Orphanet Journal of Rare Diseases, vol. 7, 70 . https://doi.org/10.1186/1750-1172-7-70
Orphanet Journal of Rare Diseases
Background Arteriosclerosis and emphysema develop in individuals with Schimke immuno-osseous dysplasia (SIOD), a multisystem disorder caused by biallelic mutations in SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff0e0995712e817e2e461d654ddc339
https://lirias.kuleuven.be/handle/123456789/653703
https://lirias.kuleuven.be/handle/123456789/653703
Publikováno v:
Current Genomics
Traditionally eukaryotic genes are considered independently expressed under the control of their promoters and cis-regulatory domains. However, recent studies in worms, flies, mice and humans have shown that genes co-habiting a chromatin domain or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d637aaf7f9aed3ad9815ef75df35af
https://pubmed.ncbi.nlm.nih.gov/19721813
https://pubmed.ncbi.nlm.nih.gov/19721813
Autor:
Leah I. Elizondo, Sandrine Willaime-Morawek, Ryuki Hirano, Kimiko Deguchi, Thomas Lücke, Hideyuki Okano, Emily A. Sloan, Cheng Huang, Ralph D. Powell, Yonehiro Kanemura, Katja M. Marwedel, Ken Inoue, Karen Santa Cruz, Jennifer L. Northrop, Johanna Marietta Clewing, Dawna L. Armstrong, Derek van der Kooy, Cornelius F. Boerkoel, Kunho Choi, Shu Lou
Publikováno v:
Journal of neuropathology and experimental neurology. 67(6)
Schimke immuno-osseous dysplasia (OMIM 242900) is an uncommon autosomal-recessive multisystem disease caused by mutations in SMARCAL1 (swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like 1), a gene encoding a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::466b37515440dcfc7c49de03a5f8be8e
https://pubmed.ncbi.nlm.nih.gov/18520775
https://pubmed.ncbi.nlm.nih.gov/18520775
Autor:
Dominique Bonneau, Asbjørg Stray-Pedersen, Nathalie Biebuyck-Gouge, Georges Deschênes, Nihal Özdemir, Barbara Hinkelmann, Sandra Cockfield, Stavroula Psoni, Guiliana Lama, David V. Milford, Maria Kanariou, Helen Fryssira, Anja Stein, Lawrence R. Shoemaker, Silvia Majore, Sarah F. Smithson, Natasa Stajic, Isabel Cordeiro, Onur Sakallioglu, Belde Kasap, Helen Georgaki, Beate Schmidt, Valérie Cormier-Daire, Newton A C S Wong, Bertram F. Pontz, Radovan Bogdanovic, Flora Sotsiou, Encarna Guillén-Navarro, Doris Taha, Cornelius F. Boerkoel, Graham Smith, Sara Sebnem Kilic, Kunho Choi, Stefan Fründ, Karel Cutka, J. Marietta Clewing, Shu Lou, Petra Lamfers, Karlien Cransberg, Emily A. Sloan, Pierre Cochat, Yumi Asakura, Chantal Loirat, Jochen H. H. Ehrich, Denis Morin, Jane Tizard, Herbert Reichenbach, David Goodman, Michel Tsimaratos, Cristina Rusu, Laure Collard, Harika Alpay, Yan Huang, Jorge M. Saraiva, Sabine Sigaudy, Willem Proesmans, Thomas Lücke, Sophie Taque, Jean Luc André, Caterina Cancrini, Silke Reif
Schimke immunoosseous dysplasia (SIOD), which is characterized by prominent spondyloepiplayseal dysplasia, T-cell deficiency, and focal segmental glomerulosclerosis, is a panethnic autosomal recessive multisystem disorder with variable expressivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a509839dac6bcb390f642383f690409f
https://avesis.deu.edu.tr/publication/details/da3be966-7ee9-4d6f-a09b-18e79d6dbac2/oai
https://avesis.deu.edu.tr/publication/details/da3be966-7ee9-4d6f-a09b-18e79d6dbac2/oai
Autor:
Johanna Marietta Clewing, Dimitrios Tsikas, Cornelius F. Boerkoel, Thomas Lücke, J. H. H. Ehrich, Nele Kanzelmeyer, Anibh M. Das, Bernhard Vaske
Publikováno v:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 38(10)
Schimke-immuno-osseous dysplasia (SIOD) is an autosomal recessive disorder with the main clinical findings of spondyloepiphyseal dysplasia, nephrotic syndrome, and defective cellular immunity. Vaso-occlusive processes, especially generalized atherosc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::420a9938102c7b2b3addfa9ea9bd5438
https://pubmed.ncbi.nlm.nih.gov/17075778
https://pubmed.ncbi.nlm.nih.gov/17075778