Concepedia

Author

H. K. Harms

Universitätskinderklinik

Also Known As

H HARMS, H Harms, H K Harms, H Karsten Harms, H. Harms, H. K. Harms, H. Karsten Harms, H.K Harms, H.K. Harms, Hinrich Karsten Harms

44

Publications

2.1K

Citations

19

H-Index

52

Concepts

All Affiliations

UniversitätskinderklinikRoche (Switzerland)Cystic Fibrosis Research FoundationRoyal Brompton HospitalHôpital Robert-Debré
HK

About

H. K. Harms is an author at Universitätskinderklinik specializing in medicine, pathology, and diabetes.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

8

8

912

2

Allergy

2

2

92

3

Health Sciences

1

1

11

4

Natural Sciences

1

1

427

5

Public Health

1

1

11

H. K. Harms

×

20

Publications

2K

Citations

17

H-Index

YearCitations

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.

R Niehues, Martin Hasilik, Gordon Alton,

Journal of Clinical Investigation

1998

427

Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study

G. Mastella, Maurizio Rainisio, H. K. Harms,

European Respiratory Journal

2000

240

Presence of cystic fibrosis‐related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: Data from the European Epidemiologic Registry of Cystic Fibrosis

Christian Koch, Maurizio Rainisio, U. Madessani,

Pediatric Pulmonology

2001

215

The diagnosis of coeliac disease. A commentary on the current practices of members of the European Society for Paediatric Gastroenterology and Nutrition (ESPGAN).

A S McNeish, H. K. Harms, J-B Rey,

Archives of Disease in Childhood

1979

209

European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations

Christian Koch, H. Cuppens, Maurizio Rainisio,

Pediatric Pulmonology

2001

195

Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF

J Navarro, Maurizio Rainisio, H. K. Harms,

European Respiratory Journal

2001

169

Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency

H. K. Harms, KP Zimmer, Karin Kurnik,

Acta Paediatrica

2002

73

International practice patterns by age and severity of lung disease in cystic fibrosis: Data from the epidemiologic registry of cystic fibrosis (ERCF)

Christian Koch, Sheila G. McKenzie, Haley Kaplowitz,

Pediatric Pulmonology

1997

67

A reliable screening test for childhood celiac disease: Fluorescent immunosorbent test for gliadin antibodies

Annemarie Bürgin-Wolff, R.M. Bertele, R. Berger,

The Journal of Pediatrics

1983

58

Correlation of IgE antibody titer to <i>Aspergillus fumigatus</i> with decreased lung function in cystic fibrosis

T. Nicolai, Sissi Arleth, Anne Spaeth,

Pediatric Pulmonology

1990

51

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