H. Hadorn

发表

MRI of primary meningeal sarcomas in two children: differential diagnostic considerations

S. Weis, K. Hahn, J. Egger, 1997, Neuroradiology.

Alpha-1-antitrypsin deficiency in children: liver disease is not reflected by low serum levels of alpha-1-antitrypsin - a study on 48 pediatric patients.

T. Lang, H. Hadorn, M. Mühlbauer, 2005, European journal of medical research.

Reduced incidence of severe metabolic crisis or death in children with medium chain acyl-CoA dehydrogenase deficiency homozygous for c.985A>G identified by neonatal screening.

I. Knerr, B. Liebl, U. Nennstiel-Ratzel, 2005, Molecular genetics and metabolism.

Mutation analysis in the diagnosis of cystic fibrosis

T. Meitinger, J. Rosenecker, T. Deufel, 1993, European Journal of Pediatrics.

Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase.

E. Auerswald, I. Assfalg-Machleidt, W. Machleidt, 1995, FEBS letters.

Replacement therapy for a homozygous protein C deficiency‐state using a concentrate of human protein C and S

H. Engelmann, P. Knöbl, K. Auberger, 1988, British journal of haematology.

Hormone-elicited enzyme release by the small intestinal wall

R. Portmann, J. Adelson, H. Hadorn, 1972, Gut.

Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria

A. Roscher, D. Applegarth, B. Rolinski, 2000, Journal of Inherited Metabolic Disease.

Bicarbonate in cystic fibrosis.

R. Schreiber, K. Kunzelmann, H. Hadorn, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Crohn's disease and ulcerative colitis with onset in the same year in two sisters.

V. Lucidi, M. Castro, H. Hadorn, 1996, Journal of pediatric gastroenterology and nutrition.

Pretransplant management and small bowel-liver transplantation in an infant with microvillus inclusion disease.

J. Vanderhoof, A. Langnas, A. Phillips, 1998, Journal of pediatric gastroenterology and nutrition.

Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia.

W. Kiess, M. le Merrer, A. Phillips, 1999, Journal of pediatric gastroenterology and nutrition.

Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.

A. Holzinger, P. Mayerhofer, A. Roscher, 2002, American journal of human genetics.

Renal function and renotropic effects of secretin in cystic fibrosis.

L. Tsui, K. Schärer, F. Schaefer, 1997, European journal of medical research.

Vitamin D dependent rickets type II with myelofibrosis and immune dysfunction

B. Belohradsky, H. Hadorn, K. Kruse, 1991, European Journal of Pediatrics.

Interferon alpha-2a therapy of consumptive coagulopathy in Kasabach-Merritt syndrome

M. Hauser, H. Hadorn, C. Klein, 1992, European Journal of Pediatrics.

Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to

E. Auerswald, I. Assfalg-Machleidt, W. Machleidt, 1995 .

Activation of Human Pancreatic Proteolytic Enzymes: The Role of Enteropeptidase and Trypsin

A. Freiburghaus, H. Hadorn, J. Roduner, 2021, JPGN reports.

Hartnup syndrome, progressive encephalopathy and allo-albuminaemia

N. Herschkowitz, K. Schmidtke, W. Endres, 1992, European Journal of Pediatrics.

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria

M. Durán, K. Gibson, T. Deufel, 1993, European Journal of Pediatrics.

A recombinant polypeptide model of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator is a GTP‐binding protein

E. Auerswald, P. Neth, W. Machleidt, 1996, FEBS letters.

Fetal alcohol syndrome and malignant disease

O. Linderkamp, W. Kiess, R. Haas, 1984, European Journal of Pediatrics.