Zobrazeno 1 - 10 of 27 pro vyhledávání: '"H. B. Hadorn"'
1
MRI of primary meningeal sarcomas in two children: differential diagnostic considerations
Autor: Joseph Egger, H. B. Hadorn, Sabine Weil, Serge Weis, Klaus Hahn, Thomas Pfluger, K. Bise
Publikováno v: Neuroradiology. 39:225-228
Meningeal sarcomas are very rare, highly aggressive tumours affecting children more frequently than adults. The clinical course and MRI of meningeal sarcomas in two cases are discussed with special regard to possible misinterpretation. In one case MR
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b20a240d8d20b2ca748fa7a33597921d
https://doi.org/10.1007/s002340050399
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4
Renal function and renotropic effects of secretin in cystic fibrosis
Autor: D, Windstetter, F, Schaefer, K, Schärer, K, Reiter, R, Eife, H K, Harms, R, Bertele-Harms, F, Fiedler, L C, Tsui, P, Reitmeir, M, Horster, H B, Hadorn
Publikováno v: European journal of medical research. 2(10)
In ten cystic fibrosis patients and nine age-matched controls, renal function was determined before and after infusion of secretin. Under baseline conditions creatinine excretion and clearance were significantly elevated, exclusively due to those pat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a63b920bcaa42896de616b63f2ce572e
https://pubmed.ncbi.nlm.nih.gov/9348270
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5
Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase
Autor: C, Randak, A A, Roscher, H B, Hadorn, I, Assfalg-Machleidt, E A, Auerswald, W, Machleidt
Publikováno v: FEBS letters. 363(1-2)
CFTR-NBF-2 was expressed in Escherichia coli in fusion with glutathione-S-transferase, the soluble portion was purified and identified as a structured protein by its CD spectrum. Association reactions of the recombinant NBF-2 with adenine nucleotides
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::01e7a5a9a11f6f49b584f94730764b0c
https://pubmed.ncbi.nlm.nih.gov/7537226
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6
Mutation analysis in the diagnosis of cystic fibrosis
Autor: T. Deufel, K. Harms, R. Bertele-Harms, H.K Rabe, Thomas Meitinger, Adelbert A. Roscher, H.-B. Hadorn, T. Wieser, J. Rosenecker
Publikováno v: European journal of pediatrics. 152(11)
Since the characterization of the gene encoding the cystic fibrosis transmembrane conductance regulator protein and identification of its main mutation, delta F508, causing cystic fibrosis (CF), more than 150 mutations in this gene have been reported
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a12c31b0ab841426d82718fc7d716e
https://pubmed.ncbi.nlm.nih.gov/8276021
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7
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria
Autor: N. G. Kennaway, H. Ibel, Marinus Duran, Kenneth M. Gibson, T. Deufel, W. Endres, H. B. Hadorn, I. Paetzke
Publikováno v: European journal of pediatrics. 152(8)
In a 4.5-month-old boy presenting with marked muscular hypotonia in the neonatal period, hepatomegaly, cardiac hypertrophy, recurrent hypoglycemia, metabolic acidosis, and secondary carnitine deficiency, there was a considerable urinary excretion of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::034200eec08432f26bc39e4dee924934
https://pubmed.ncbi.nlm.nih.gov/7691603
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8
Vitamin D dependent rickets type II with myelofibrosis and immune dysfunction
Autor: H. B. Hadorn, K. Kruse, S. Däumling, Bernd H. Belohradsky, M. M. Walka
Publikováno v: European journal of pediatrics. 150(9)
We present a new patient with vitamin D dependent rickets type II. A 20-month-old Arabian boy whose parents are first cousins showed florid rickets, myelofibrosis and recurrent septicaemia. In addition to absent specific binding for 1,25-dihydroxyvit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625142a01e453179a99142afc8c02b63
https://pubmed.ncbi.nlm.nih.gov/1655462
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