Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Dennis J. Byrd"'
Publikováno v:
Monatsschrift Kinderheilkunde. 144:1063-1066
Primare Hyperoxalurien sind seltene angeborene Stoffwechselstorungen. Von 1978–1993 diagnostizierten wir 10 Patienten mit primarer Hyperoxalurie. Die zur Diagnose fuhrenden Symptome waren Nephrolithiasis (4), Harnwegsinfekt (2), Gedeihstorung (2) u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1f8cf56ce84419177ec76a088333e6b
https://doi.org/10.1007/s001120050066
https://doi.org/10.1007/s001120050066
Publikováno v:
Monatsschrift Kinderheilkunde. 144:1078-1086
Fragestellung: Es werden die Verlaufe von 8 Patienten mit Storungen der Harnstoffsynthese [Carbamylphosphatsynthetasemangel (4), Citrullinamie (2) und Argininosuccinatlyasemangel (2) ] beschrieben. Methode/Therapieprinzipien: Akuttherapie: Na-Benzoat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afa133cd56bc8023abdaddde672da2a1
https://doi.org/10.1007/s001120050069
https://doi.org/10.1007/s001120050069
Publikováno v:
Pediatric Nephrology. 9:39-44
We have established normal values for calcium/creatinine (Ca/Cr) and oxalate/creatinine (Ox/Cr) ratios in 25 infants (aged 1–7 days) and 391 children (aged 1 month to 14.5 years) and compared these with values obtained in 137 children with post-glo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3cd9393afe4c855880848dc1fcd9c9d
https://doi.org/10.1007/bf00858966
https://doi.org/10.1007/bf00858966
Publikováno v:
Clinica Chimica Acta. 231:61-68
The F1F0-ATPase activity of mitochondrial complex V can be rapidly measured in sonicated preparations of monolayer skin fibroblast cultures from children. We show that direct regulation at the level of ATP-synthase occurs in these cell preparations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74392b4a92c39bf3aadbca7b7a5d7fc9
https://doi.org/10.1016/0009-8981(94)90254-2
https://doi.org/10.1016/0009-8981(94)90254-2
Autor:
Johannes Brodehl, Dennis J. Byrd, Raymund Zinck, Michael Domanetzki, Arend Bökenkamp, Gerhard Schumann
Publikováno v:
Clinical Chemistry. 45:1866-1868
Cystatin C, a cationic 13.3-kDa protein (1) has recently been described as a promising endogenous marker of glomerular filtration rate (GFR) (2) in both adults (2)(3) and children (4)(5). Correlation of serum cystatin C concentrations with the result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::147b6e35a3df38c0ad29bf8b8fc40218
https://doi.org/10.1093/clinchem/45.10.1866
https://doi.org/10.1093/clinchem/45.10.1866
Autor:
Arend Bökenkamp, Gerhard Schumann, Michael Domanetzki, Raymund Zinck, Johannes Brodehl, Dennis J. Byrd
Publikováno v:
Pediatrics. 101(5)
Objectives. Serum creatinine is the most common endogenous marker of renal function. The proportionality between creatinine production and muscle mass requires adjustment for height and body composition. The low molecular weight protein cystatin C is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6051d89c28cd71088204ff90998001fd
https://pubmed.ncbi.nlm.nih.gov/9565418
https://pubmed.ncbi.nlm.nih.gov/9565418
Autor:
Gusztáv Stubnya, Tivadar Tulassay, Gabriel Miltényi, György Reusz, Dennis J. Byrd, András Szabó, Csaba Horváth, Ferenc Péter
Publikováno v:
Pediatric nephrology (Berlin, Germany). 11(5)
The impact of recombinant human growth hormone (rhGH) treatment on growth, bone mineral metabolism, and bone mineral density (BMD) was evaluated in six children (3 girls, 3 boys) with familial hypophosphatemic rickets (XLH). Five were prepubertal (ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01438105beda7bb39746b293c4588001
https://pubmed.ncbi.nlm.nih.gov/9323282
https://pubmed.ncbi.nlm.nih.gov/9323282
Autor:
David Valle, Jean-Paul Bonnefont, Friedrich K. Trefz, S. Lane Rutledge, Jean-Marie Saudubray, Christine Vianey‐Liaud, Claude Sansaricq, Galen N. Breningstall, Charles A. Stanley, William R. Treem, Warren D. Grover, Dennis J. Byrd, Paul M. Coates, Ingrid Tein, Morey W. Haymond, Susan Deleeuw, P. Divry, Rebecca S. Wappner
Publikováno v:
Annals of neurology. 30(5)
A defect in intracellular uptake of carnitine has been identified in patients with severe carnitine deficiency. To define the clinical manifestations of this disorder, the presenting features of 15 affected infants and children were examined. Progres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a70670f21829a3b94abebf7a1f6e9137
https://pubmed.ncbi.nlm.nih.gov/1763895
https://pubmed.ncbi.nlm.nih.gov/1763895
Publikováno v:
European Journal of Pediatrics. 152:1048-1049
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::422e875894c8c10ba078f294b230ec8f
https://doi.org/10.1007/bf01957239
https://doi.org/10.1007/bf01957239
Publikováno v:
Pediatric Nephrology. 5:619-619
We present results for laboratory screening and diagnostic tests--cyanide-nitroprusside test, semi-quantitative thin-layer chromatography, and quantitative amino acid column chromatography--of 43 patients with classic cystinuria. We report the effica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ff277027d95648ef7dd4ba214970bb
https://doi.org/10.1007/bf00856655
https://doi.org/10.1007/bf00856655