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Predictors of deterioration of lung function in cystic fibrosis

Pediatric pulmonology, 2002-06, Vol.33 (6), p.483-491

2002

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Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions

Biochemical journal, 1999-12, Vol.344 Pt 2 (2), p.321-330

1999

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Survey of the pre-school child health surveillance programme in Sweden

Acta Paediatrica, 2000-08, Vol.89 (s434), p.2-7

Kornfält, R

2000

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Identifying children at risk for language impairment: screening of communication at 18 months

Acta Paediatrica, 2003-09, Vol.92 (9), p.1090-1095

2003

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Pharmaceutical intervention in the care of cystic fibrosis patients

Journal of clinical pharmacy and therapeutics, 2000-12, Vol.25 (6), p.427-434

2000

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Recurrent Pseudomonas bronchopneumonia and other symptoms as in cystic fibrosis in a child with type I pseudohypoaldosteronism

Acta Paediatrica, 1998-04, Vol.87 (4), p.472-474

1998

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Identifying children at risk for language impairment: screening of communication at 18 months Reply

Acta Paediatrica, 2004-04, Vol.93 (4), p.574-575

2004

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Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden

Clinical genetics, 1999-10, Vol.56 (4), p.318-322

1999

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Utilization of Primary Care versus Specialized Care in Children with and without Chronic Illness: A Population-Based Study

Acta Paediatrica, 1991-05, Vol.80 (5), p.534-541

1991

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Cystic fibrosis caused by homozygosity for the CFTR gene mutation 175insT

Acta Paediatrica, 1995-10, Vol.84 (10), p.1199-1200

1995

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Quality in child healthcare. The views of mothers and public health nurses

Scandinavian journal of caring sciences, 1998-01, Vol.12 (4), p.195-204

1998

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Recurrent Acute Otitis Media: A Prospective Study of Children during the First Three Years of Life

Acta oto-laryngologica, 1989, Vol.107 (1-2), p.111-119

1989

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Evaluation of screening procedures for congenital cataracts

Acta Paediatrica, 2003-01, Vol.92 (12), p.1468-1473

2003

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Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I

Clinical genetics, 1998-05, Vol.53 (5), p.383-386

1998

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Cystic fibrosis mutations in southern Sweden: relationship to clinical severity

Acta Paediatrica, 1992-03, Vol.81 (3), p.262-263

1992

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Treatment Failure in Acute Otitis Media: A Clinical Study of Children during Their First Three Years of Life

Acta oto-laryngologica, 1989, Vol.108 (3-4), p.253-258

1989

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Chronic Illness among Children in a Total Population: An Epidemiological Study in a Swedish Primary Health Care District

Scandinavian journal of social medicine, 1987, Vol.15 (2), p.87-97

1987

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Behavioural Assessments in the School Health Service: A Comparison of Information Obtained from Interviews with Parents, Teachers and Children

Scandinavian journal of social medicine, 1981-01, Vol.9 (3), p.81-89

Kornfält, Ragnhild

1981

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C1q and C1 Subcomponent Complexes in Otitis-Prone and Non-Otitis-Prone Children A Prospective Study of Children during their First Years of Life

Acta Paediatrica, 1989-11, Vol.78 (6), p.911-917

1989

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Identifying children at risk for language impairment: screening of communication at 18 months

Acta Paediatrica, 2003-09, Vol.92 (9), p.1090-1095

2003

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Acute Respiratory Tract Infections in Early Childhood

Acta oto-laryngologica, 1992, Vol.112 (S492), p.72-74

1992

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Long-term Effects of Physical Exercise on Working Capacity and Pulmonary Function in Cystic Fibrosis

Acta Paediatrica, 1987-01, Vol.76 (1), p.70-75

1987

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Lung function in cystic fibrosis: acute effect of salbutamol

Respiration, 1980, Vol.40 (4), p.226

1980

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Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the α-subunit of the epithelial sodium channel

The Journal of pediatrics, 1999-12, Vol.135 (6), p.739-745

1999

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FIBRINOLYSIS IN LYMPHANGIOMA

Acta Paediatrica, 1973-09, Vol.62 (5), p.538-542

1973

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Predictors of deterioration of lung function in cystic fibrosis

Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions

Survey of the pre-school child health surveillance programme in Sweden

Identifying children at risk for language impairment: screening of communication at 18 months

Pharmaceutical intervention in the care of cystic fibrosis patients

Recurrent Pseudomonas bronchopneumonia and other symptoms as in cystic fibrosis in a child with type I pseudohypoaldosteronism

Identifying children at risk for language impairment: screening of communication at 18 months Reply

Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden

Utilization of Primary Care versus Specialized Care in Children with and without Chronic Illness: A Population-Based Study

Cystic fibrosis caused by homozygosity for the CFTR gene mutation 175insT

Quality in child healthcare. The views of mothers and public health nurses

Recurrent Acute Otitis Media: A Prospective Study of Children during the First Three Years of Life

Evaluation of screening procedures for congenital cataracts

Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I

Cystic fibrosis mutations in southern Sweden: relationship to clinical severity

Treatment Failure in Acute Otitis Media: A Clinical Study of Children during Their First Three Years of Life

Chronic Illness among Children in a Total Population: An Epidemiological Study in a Swedish Primary Health Care District

Behavioural Assessments in the School Health Service: A Comparison of Information Obtained from Interviews with Parents, Teachers and Children

C1q and C1 Subcomponent Complexes in Otitis-Prone and Non-Otitis-Prone Children A Prospective Study of Children during their First Years of Life

Identifying children at risk for language impairment: screening of communication at 18 months

Acute Respiratory Tract Infections in Early Childhood

Long-term Effects of Physical Exercise on Working Capacity and Pulmonary Function in Cystic Fibrosis

Lung function in cystic fibrosis: acute effect of salbutamol

Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the α-subunit of the epithelial sodium channel

FIBRINOLYSIS IN LYMPHANGIOMA

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