Zobrazeno 1 - 10
of 363
pro vyhledávání: '"H-J Christen"'
Publikováno v:
Monatsschrift Kinderheilkunde.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90c7a56593191c25fb969fe9f8740e4b
https://doi.org/10.1007/s00112-022-01590-w
https://doi.org/10.1007/s00112-022-01590-w
Autor:
H. Eiffert, H.-J. Christen
Publikováno v:
Monatsschrift Kinderheilkunde. 167:67-79
Das klinische Bild der Neuroborreliose wird durch die akute periphere Fazialisparese und die serose Meningitis gepragt. Weitere, allerdings seltene Manifestationen sind die lymphozytare Meningoradikulitis, der Pseudotumor cerebri und der kindliche Sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9e481d466358348096f59d15967ebf5
https://doi.org/10.1007/s00112-018-0627-7
https://doi.org/10.1007/s00112-018-0627-7
Akademický článek
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Autor:
Nuria C. Bramswig, Francois V. Bolduc, Dagmar Wieczorek, Harald Surowy, Oana Caluseriu, Thomas Wieland, Tim M. Strom, N. C. L. Noel, Hermann-Josef Lüdecke, H.-J. Christen, Hartmut Engels
Publikováno v:
Human Genetics. 136:297-305
Chromatin remodeling is a complex process shaping the nucleosome landscape, thereby regulating the accessibility of transcription factors to regulatory regions of target genes and ultimately managing gene expression. The SWI/SNF (switch/sucrose nonfe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaa7206f524bf52bf9d8a97c2c9dd90a
https://doi.org/10.1007/s00439-017-1757-z
https://doi.org/10.1007/s00439-017-1757-z
Autor:
H.-J. Christen, H. Eiffert
Publikováno v:
Monatsschrift Kinderheilkunde. 167:546-546
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81afd38fcc1a3e4445c150673e31caf3
https://doi.org/10.1007/s00112-019-0702-8
https://doi.org/10.1007/s00112-019-0702-8
Autor:
T. Herberhold, S. Grunt, H. J. Christen, Benedikt Hofmeister, Steffen Berweck, Cornelia Betzler, S. Schilling, S. Moiseeva, Gerhard Kluger, C. von Stülpnagel-Steinbeis, Katrien Jansen, B. Haeckl, Edda Haberlandt, Peter Weber
Publikováno v:
Neuropediatrics. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d0c40479302435e03a56fddc8817a24
https://doi.org/10.1055/s-0036-1583620
https://doi.org/10.1055/s-0036-1583620
Publikováno v:
Monatsschrift Kinderheilkunde. 157:1128-1136
In the present study, benefits and risks of intrathecal baclofen treatment (ITB) as a palliative therapeutic procedure for children with severe disability were assessed and evaluated. Clinical data of patients, treatment effects, adverse events, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a5f2c4a83e50688fc9c17852105b26b
https://doi.org/10.1007/s00112-009-2038-2
https://doi.org/10.1007/s00112-009-2038-2
Publikováno v:
Hämostaseologie. 29:137-142
SummaryTo determine the frequency and clinical relevance of acquired von Willebrand syndrome (aVWS) due to antiepileptic therapy by valproic acid, we investigated 50 consecutive children in three neuropediatric institutions. Coagulation factors were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::905a1e4d62989075a3b0fb9b80af5111
https://doi.org/10.1055/s-0037-1617026
https://doi.org/10.1055/s-0037-1617026
Autor:
Hans Hartmann, J. Herchenbach, Frank Donnerstag, U. Stephani, Moritz Meins, H. J. Christen, P. Ledaal, M. Hagedorn, Anibh M. Das, Thomas Lücke
Publikováno v:
Neuropediatrics. 38:143-147
Alexander disease is a rare disorder of cerebral white matter due to a dysfunction of astrocytes. The most common infantile form presents as a megalencephalic leukodystrophy. Mutations of the GFAP gene, encoding Glial Fibrillary Acidic Protein, have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b61ff3a86334fab450b62884893a022
https://doi.org/10.1055/s-2007-985902
https://doi.org/10.1055/s-2007-985902
Publikováno v:
Developmental Medicine & Child Neurology. 42:122-132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea245eb6c495029ceb9fc2d907bf0eb6
https://doi.org/10.1111/j.1469-8749.2000.tb00057.x
https://doi.org/10.1111/j.1469-8749.2000.tb00057.x