Zobrazeno 1 - 10
of 43
pro vyhledávání: '"H.-P. Krohn"'
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 105:6-11
Congenital hyperthyroidism is a very rare disease. But, for each affected child it has to be considered as a serious condition because of the negative impact of hyperthyroidism on fetal and postnatal development. If the manifestation occurs during fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e8efa3d36d293fe80edc7d84ab5de4c
https://doi.org/10.1055/s-0029-1211924
https://doi.org/10.1055/s-0029-1211924
Autor:
G. H. Monrad-Krohn
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 10, Iss 2, Pp 213-220 (1952)
Externí odkaz:
https://doaj.org/article/92c2f29d4e304af88b97da38a4c779ed
Publikováno v:
Archives of Disease in Childhood. 65:1125-1128
The clinical data of 18 patients with X linked hypophosphataemia were analysed retrospectively. The height data were expressed as SD scores. There was no difference in the final height of patients treated with vitamin D (or 1,25-dihydroxyvitamin D) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1cf629b448141ebe6b411f897e829f
https://doi.org/10.1136/adc.65.10.1125
https://doi.org/10.1136/adc.65.10.1125
Autor:
B. Robin, Eric Bieth, Peter Freisinger, M. Mouchard, H. P. Krohn, Mark E Nunes, J. F. Gibrat, Anne-Sophie Lia-Baldini, Arthur S. Aylsworth, F. Muller, Etienne Mornet, B. Simon-Bouy, J.L. Serre, S. Delanote, J. C.C. Hu, Agnès Taillandier
Publikováno v:
Human genetics. 109(1)
Hypophosphatasia is an inherited disorder characterized by defective bone mineralization and a deficiency of tissue-nonspecific alkaline phosphatase (TNSALP) activity. The disease is highly variable in its clinical expression, because of various muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ce291e6d4dd54ab8d5f9e78e65ffdbc
https://pubmed.ncbi.nlm.nih.gov/11479741
https://pubmed.ncbi.nlm.nih.gov/11479741
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(5)
Gain of function mutations in the TSH receptor (TSHR) have been identified as the molecular basis for congenital and acquired forms of autonomous thyroid function. Herein, we report the molecular characterization of a case of severe congenital hypert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cddf8cce81d662e6a9dbc122112aeed3
https://pubmed.ncbi.nlm.nih.gov/9589634
https://pubmed.ncbi.nlm.nih.gov/9589634
Autor:
H. Jüppner, H.-P. Krohn
Publikováno v:
Endokrinologie des Kindes-und Jugendalters ISBN: 9783540618553
Die Einfuhrung molekularbiologischer Klonierungs- und Untersuchungsmethoden hat — in einem erstaunlich kurzen Zeitraum — das Verstandnis der calcium-regulierenden Hormonsysteme in einem auserordentlichen Ausmas verbessert. Dadurch ist es in viele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6bd46a1e28d5f34e47725a64a01defe
https://doi.org/10.1007/978-3-642-59043-6_8
https://doi.org/10.1007/978-3-642-59043-6_8
Publikováno v:
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde. 138(4)
The clinical course of 48 children (27 boys and 21 girls) with multicystic kidney dysplasia was analysed retrospectively. The patients were seen and treated at the Children's Hospital of Medical School Hannover between 1976 to 1989. There was no fami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf1d0f60ea30565032d7c9de41d0782f
https://pubmed.ncbi.nlm.nih.gov/2192270
https://pubmed.ncbi.nlm.nih.gov/2192270
Publikováno v:
Ultraschall-diagnostik ’89 ISBN: 9783642934681
Die familiare hypophosphatamische Rachitis oder Vitamin D-resistente Rachitis (VDRR) wird X-chromosomal dominant vererbt. Die Haufigkeit wird mit 1 auf 20000 angegeben. Der Erkrankung liegt ein 1 alpha Hydroxylase-Defekt der Niere zugrunde. Es besteh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c94f9e3bec03d5025b2202595e4f8bf
https://doi.org/10.1007/978-3-642-93467-4_111
https://doi.org/10.1007/978-3-642-93467-4_111
Publikováno v:
Ultraschall-diagnostik ’89 ISBN: 9783642934681
Die multizystische Nierendysplasie ist eine fruhembryonale, meist einseitige dysplastische Fehlbildung der Niere. Anstelle der Niere findet sich ein nicht ausscheidungsfahiges Zystenkonglomerat ohne erkennbares Nierenparenchym. Der Ureter und das Nie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aafbecedd436599267413b2d56ea5f9a
https://doi.org/10.1007/978-3-642-93467-4_106
https://doi.org/10.1007/978-3-642-93467-4_106
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 100:1244-1247
In three children (aged 6-8 years)acute renal failure developed three to five days after head injury. After emergency treatment and measures to prevent cerebral oedema, two of the children were given simultaneously dextran, cefalotin, gentaminic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa3c8491d0f75b08321c23789397cd78
https://doi.org/10.1055/s-0028-1106364
https://doi.org/10.1055/s-0028-1106364