Zobrazeno 1 - 10
of 141
pro vyhledávání: '"W. Tulzer"'
Autor:
Ch. Flamm, H. Sauer, K. H. Kärcher, J. Rücker, O. A. Jürgenssen, R. Kurz, Arnulf Hackl, R. Krepler, H. Haas, Ch. Urban, A. Rosenkranz, G. Reinartz, L. Howanietz, J. Hüttenberger, Krepler P, H. Hartl, Pichler E, H. Messner, P. Wurnig, W. Tulzer, U. Busch, Kaulfersch W, G. Menardi, E. Kahr, G. Hubmer, Ingomar Mutz, G. Brandesky, F. Helmer, W. Esch
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 106:1248-1253
Uniform treatment based on the therapeutic approach of the 1st and 2nd US National Wilms' Tumor Study was decided on in March 1976 by paediatricians, surgeons, urologists and radiotherapists in Austria. Wilms' tumour was diagnosed in 34 children betw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58765165861f867c60bd83dfb66e2560
https://doi.org/10.1055/s-2008-1070491
https://doi.org/10.1055/s-2008-1070491
Publikováno v:
Klinische Pädiatrie. 204:123-125
This is a report about a phenotypical normal girl with nephropathy and gonadal dysgenesis. At the age of 2 years 8 months she presented with steroid resistant nephrotic syndrome. Focal segmental glomerulosclerosis was found by biopsy. Because of dela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62888d65d77027952fe3fa9943500b77
https://doi.org/10.1055/s-2007-1025336
https://doi.org/10.1055/s-2007-1025336
Publikováno v:
Klinische Pädiatrie. 202:117-119
Maternal virilization association with the birth of a virilized female infant has been reported in gravidas with luteoma. We describe a similar case with ambiguous genitalia (type Prader III). The only pathological finding was an elevated postpartum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be407fde2d57b4b390596529a89dfab2
https://doi.org/10.1055/s-2007-1025502
https://doi.org/10.1055/s-2007-1025502
Publikováno v:
Pediatric cardiology. 15(1)
A 20-month-old girl with massive digitoxin intoxication (initial digitoxin serum level: 629 ng/ml) was successfully treated with digoxin-specific antibody fragments (Fab). She presented with moderate signs of digitalis toxicity (somnolence, bradycard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce5f1577833a45e898bf9503d4d26040
https://pubmed.ncbi.nlm.nih.gov/8115274
https://pubmed.ncbi.nlm.nih.gov/8115274
Publikováno v:
Wiener klinische Wochenschrift. 105(11)
An eleven month-old boy presented clinically with craniofacial dysmorphia, severe psychomotor retardation, neurological deterioration, no response to visual and acoustic stimuli, failure to thrive, hepatomegaly and adrenal insufficiency. Specific bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::53960f90b89461cbad0a6f581448dd4c
https://pubmed.ncbi.nlm.nih.gov/7687405
https://pubmed.ncbi.nlm.nih.gov/7687405
Publikováno v:
Klinische Padiatrie. 204(2)
This is a report about a phenotypical normal girl with nephropathy and gonadal dysgenesis. At the age of 2 years 8 months she presented with steroid resistant nephrotic syndrome. Focal segmental glomerulosclerosis was found by biopsy. Because of dela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89ce8d0d5c6759dc9d4c7aabdbd2c15a
https://pubmed.ncbi.nlm.nih.gov/1583852
https://pubmed.ncbi.nlm.nih.gov/1583852
Publikováno v:
Padiatrie und Padologie. 27(6)
The etiology of Schoenlein-Henoch' Syndrome has not yet been fully clarified [10, 15]. An allergically toxic genesis is under discussion [8, 19]. The classical combination of symptoms consists of urticariel efflorescences, bleeding of skin and lining
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d21f790b32dfbc98bcb2bb62e13e7242
https://pubmed.ncbi.nlm.nih.gov/1484711
https://pubmed.ncbi.nlm.nih.gov/1484711
Publikováno v:
Wiener medizinische Wochenschrift (1946). 142(10)
A 15 month old girl with suspected immune neutropenia was treated with high dose immunoglobulin because of recurrent infections over a period of 9 months. Before therapy her neutrophil counts were below 0.5 G/l. With monthly intravenous immunoglobuli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35fc142c4c9f6df3ff579148c12167e9
https://pubmed.ncbi.nlm.nih.gov/1514300
https://pubmed.ncbi.nlm.nih.gov/1514300
Publikováno v:
Wiener klinische Wochenschrift. 104(11)
Two HLA-identical sisters have developed the full picture of type I polyglandular autoimmune syndrome over a period of 12 years. Both girls have hypoparathyroidism and Addison's disease. One of them additionally developed diabetes mellitus, hypergona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f9320084858c9a31c54eab6514645b6b
https://pubmed.ncbi.nlm.nih.gov/1621394
https://pubmed.ncbi.nlm.nih.gov/1621394
Autor:
K, Schmitt, W, Tulzer
Publikováno v:
Padiatrie und Padologie. 26(4)
In beta thalassaemia patients the subcutaneous desferrioxamine chelation therapy is performed routinely. Rare indications are hypoplastic anaemia, congenital dyserythropoetic anaemia and Fanconi anaemia. We initiated the chelation agent in three pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::070ae1b379606868bc691433bb7a257b
https://pubmed.ncbi.nlm.nih.gov/1749630
https://pubmed.ncbi.nlm.nih.gov/1749630