Zystische Fibrose und Zöliakie : Zwei FallbeschreibungenSANTER, R; HARMS, H. K.Monatsschrift für Kinderheilkunde. 1990, Vol 138, Num 9, pp 623-626, issn 0026-9298Article

Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiencyHARMS, H. K; ZIMMER, K-P; KURNIK, K et al.Acta paediatrica (Oslo). 2002, Vol 91, Num 10, pp 1065-1072, issn 0803-5253, 8 p.Article

European Epidemiologic Registry of Cystic Fibrosis (ERCF) : Comparison of major disease manifestations between patients with different classes of mutationsKOCH, C; CUPPENS, H; RAINISIO, M et al.Pediatric pulmonology. 2001, Vol 31, Num 1, pp 1-12, issn 8755-6863Article

Multicenter, open-label study of recombinant human dnase in cystic fibrosis patients with moderate lung diseaseHARMS, H. K; MATOUK, E; KOLBE, J et al.Pediatric pulmonology. 1998, Vol 26, Num 3, pp 155-161, issn 8755-6863Article

The fluorescent immunosorbent test for IgG gliadin antibodies and the leucocyte migration inhibition test in coeliac disease; comparison of diagnostic valueBERTELE, R. M; BÜRGIN-WOLFF, A; BERGER, R et al.European journal of pediatrics. 1985, Vol 144, Num 1, pp 58-62, issn 0340-6199Article

Does optimal egg size vary with demographic stage because of a physiological constraint?BOWDEN, R. M; HARMS, H. K; PAITZ, R. T et al.Functional ecology (Print). 2004, Vol 18, Num 4, pp 522-529, issn 0269-8463, 8 p.Article

Geographic distribution and origin of CFTR mutations in GermanyTÜMMLER, B; STORRS, T; RUTJES, J et al.Human genetics. 1996, Vol 97, Num 6, pp 727-731, issn 0340-6717Article

Genetic determination of diabetes mellitus in patients with cystic fibrosisROSENECKER, J; EICHLER, I; KÜHN, L et al.The Journal of pediatrics. 1995, Vol 127, Num 3, pp 441-443, issn 0022-3476Article

Diversity of the basic defect of homozygous CFTR mutation genotypes in humansSTANKE, F; BALLMANN, M; GRIESE, M et al.Journal of medical genetics. 2008, Vol 45, Num 1, pp 47-54, issn 0022-2593, 8 p.Article

Factors associated with poor pulmonary function : cross-sectional analysis of data from the ERCFNAVARRO, J; RAINISIO, M; HARMS, H. K et al.The European respiratory journal. 2001, Vol 18, Num 2, pp 298-305, issn 0903-1936Article

A paediatric Crohn's disease activity index (PCDAI). Is it useful ?HARMS, H. K; BLOMER, R; BERTELE-HARMS, R.-M et al.Acta paediatrica. Supplement. 1994, Vol 83, Num 395, pp 22-26, issn 0803-5326Article

Correlation of IgE antibody titer to Aspergillus fumigatus with decreased lung function in cystic fibrosisNICOLAI, T; ARLETH, S; SPAETH, A et al.Pediatric pulmonology. 1990, Vol 8, Num 1, pp 12-15, issn 8755-6863Article

Calcium metabolism and cystic fibrosis: mitochondrial abnormalities suggest a modification of the mitochondrial membraneVON RUECKEL, A. A; BERTELE, R; HARMS, H. K et al.Pediatric research. 1984, Vol 18, Num 7, pp 594-599, issn 0031-3998Article

Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiencyHARMS, H.-K; BERTELE-HARMS, R.-M; BRUER-KLEIS, D et al.The New England journal of medicine. 1987, Vol 316, Num 21, pp 1306-1309, issn 0028-4793Article