Search Results - "Nützenadel, W"

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    Rectal biopsy for diagnosis of intestinal neuronal dysplasia in children: a prospective multicentre study on interobserver variation and clinical outcome by Koletzko, S, Jesch, I, Faus-Keβler, T, Briner, J, Meier-Ruge, W, Müntefering, H, Coerdt, W, Wessel, L, Keller, K M, Nützenadel, W, Schmittenbecher, P, Holschneider, A, Sacher, P

    Published in Gut (01-06-1999)
    “…BACKGROUND Intestinal neuronal dysplasia (IND) of the colonic submucous plexus is considered to be a congenital malformation of the enteric nervous system…”
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    Life-Threatening Parvovirus B19-Associated Myocarditis and Cardiac Transplantation as Possible Therapy: Two Case Reports by Enders, G., Dötsch, J., Bauer, J., Nützenadel, W., Hengel, H., Haffner, D., Schalasta, G., Searle, K., Brown, K. E.

    Published in Clinical infectious diseases (01-02-1998)
    “…Parvovirus B19 infection can cause a wide spectrum of disease syndromes. Two cases of parvovirus B19 infection were identified that resulted in…”
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    Malignant osteopetrosis obscured by maternal vitamin D deficiency in a neonate by Popp, D, Zieger, B, Schmitt-Gräff, A, Nützenadel, W, Schaefer, F

    Published in European journal of pediatrics (01-06-2000)
    “…A neonate presented with clinical, biochemical, endocrine and radiographic features consistent with vitamin D deficiency rickets of maternal origin. Persistent…”
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    Pulmonary alveolar lipoproteinosis in a seven-year-old girl. A follow-up over six years by Paul, K, Müller, K M, Oppermann, H C, Nützenadel, W

    Published in Acta pædiatrica Scandinavica (01-04-1991)
    “…Alveolar lipoproteinosis is a rare disease in childhood, and its outcome is considered unfavourable compared to adults. We report on the spontaneous…”
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    Effects of Indomethacin in Congenital Chloride Diarrhea by Mayatepek, Ertan, Seyberth, Hannsjörg W, Nützenadel, Walter

    “…SUMMARYClinical and biochemical effects of indomethacin were monitored in a patient with congenital chloride diarrhea (CCD) before and after 10 days of…”
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    Fanconi-Bickel syndrome by Manz, F, Bickel, H, Brodehl, J, Feist, D, Gellissen, K, Geschöll-Bauer, B, Gilli, G, Harms, E, Helwig, H, Nützenadel, W

    Published in Pediatric nephrology (Berlin, West) (01-07-1987)
    “…Clinical, biochemical, functional and morphological data are presented in nine infants, children and adults, with Fanconi-Bickel syndrome. Long-term follow-up…”
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    Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type I by Mayatepek, E., Schröder, M., Kohlmüller, D., Bieger, WP, Nützenadel, W.

    Published in Acta Paediatrica (01-10-1997)
    “…The effects on isoelectrofocusing patterns of serum glycoproteins were studied in a patient with CDG syndrome type I and phosphomannomutase deficiency during 3…”
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    Partial trisomy 22 and 11 due to a paternal 11;22 translocation associated with Hirschsprung disease by BEEDGEN, B, NÜTZENADEL, W, QUERFELD, U, WEISS-WICHERT, P

    Published in European journal of pediatrics (01-08-1986)
    “…The 11;22 translocation seems to be the most frequent, non-Robertsonian, translocation in man. Approximately 50 cases with an unbalanced karyotype 47,XX (or…”
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    Absorption of free and peptide-linked glycine and phenylalanine in children with active celiac disease by Nützenadel, W, Fahr, K, Lutz, P

    Published in Pediatric research (01-04-1981)
    “…Using a marker perfusing technique, the jejunal absorption rates of glycine and phenylalanine from test solutions containing either the free amino acids or…”
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    Metabolic Fate of Free and Peptide‐Linked Phenylalanine During Infusion into Portal or Femoral Vein of Rats by Niitzenadel, W., Fahr, K., Schwartze, E.

    “…Summary [14C]Phenylalanine, either as free amino acid or as glycylphenylalanine, was continuously infused over 3 h into the portal or femoral vein of…”
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    The effect of jejunectomy on alkaline phosphatase activity in the ileum by Gawlik, Z, Nützenadel, W, Krawczyk, M, Wiśniewska, I E

    “…The activity of alkaline phosphatase activity in the small intestinal wall was studied in dogs after jejunectomy. The observations were made 3, 6, 8 or 9 and…”
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    Sclerosis of the intestinal tract with severe malabsorption by Nützenadel, W, Fahr, K, Daum, R, Herrmann, R

    Published in European Journal of Pediatrics (01-01-1977)
    “…The clinical findings and pathological changes in a 14 year old boy who died from severe malabsorption are presented. Early signs of the illness were attacks…”
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    Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush border by Manz, F, Waldherr, R, Fritz, H P, Lutz, P, Nützenadel, W, Reitter, B, Schärer, K, Schmidt, H, Trefz, F

    Published in Clinical nephrology (01-09-1984)
    “…In a girl with idiopathic de Toni-Debré-Fanconi syndrome associated with psychomotor retardation, severe renal tubular dysfunction was observed from the first…”
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    Motility malfunction of the gastrointestinal tract by rare diseases--fibrosis of the intestinal wall by Daum, R, Nützenadel, W, Roth, H, Zachariou, Z

    Published in Progress in pediatric surgery (1989)
    “…We report on two children who were admitted with chronic ileus without mechanical obstruction. In the 4-month-old female newborn, high-dose radiation was…”
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