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Infection with Burkholderia cepacia Complex Genomovars in Patients with Cystic Fibrosis: Virulent Transmissible Strains of Genomovar III Can Replace Burkholderia multivorans

Clinical infectious diseases, 2001-11, Vol.33 (9), p.1469-1475

2001

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Epidemiology of Pseudomonas aeruginosa in Cystic Fibrosis in British Columbia, Canada

American journal of respiratory and critical care medicine, 2002-10, Vol.166 (7), p.988-993

2002

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An unusual presentation of doxycycline-induced photosensitivity

Pediatrics (Evanston), 2000-07, Vol.106 (1), p.E13-e13

2000

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Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy

Journal of inherited metabolic disease, 2004-01, Vol.27 (6), p.778-780

2004

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Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiency

Pediatric research, 1986-03, Vol.20 (3), p.274-279

1986

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A genomic approach to mutation analysis of holocarboxylase synthetase gene in three Chinese patients with late-onset holocarboxylase synthetase deficiency

Clinical biochemistry, 2003-03, Vol.36 (2), p.145-149

2003

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Treatment of recurrent hemoptysis in a child with cystic fibrosis by repeated bronchial artery embolizations and long-term tranexamic acid

Pediatric pulmonology, 1996-10, Vol.22 (4), p.275-279

1996

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Orthotopic liver transplantation in a patient with carbamyl phosphate synthetase deficiency and cystic fibrosis

Paediatrics & child health, 2003-10, Vol.8 (8), p.497-498

2003

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Selective media for isolation of Burkholderia (Pseudomonas) cepacia from the respiratory secretions of patients with cystic fibrosis

Journal of clinical pathology, 1995-05, Vol.48 (5), p.488-490

1995

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Bone marrow transplantation in Gaucher's disease : effect of mixed chimeric state

Bone marrow transplantation (Basingstoke), 1994-08, Vol.14 (2), p.327-330

1994

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Cardiomyopathy associated with nonendemic selenium deficiency in a Caucasian adolescent

The American journal of clinical nutrition, 1990-09, Vol.52 (3), p.572-577

1990

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Pseudomonas aeruginosa colonization of the gastrointestinal tract in patients with cystic fibrosis

The Journal of infectious diseases, 1993-01, Vol.167 (1), p.226-229

1993

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Allelic association and linkage studies in Wilson disease

Human molecular genetics, 1993-09, Vol.2 (9), p.1401-1405

1993

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The high incidence of valproate hepatotoxicity in infants may relate to familial metabolic defects

Canadian journal of neurological sciences, 1990-05, Vol.17 (2), p.145-148

1990

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Biochemical investigation of a child with molybdenum cofactor deficiency

Clinical biochemistry, 1990-12, Vol.23 (6), p.537-542

1990

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Communicability of Pseudomonas infections in patients with cystic fibrosis

The Journal of pediatrics, 1989-06, Vol.114 (6), p.1068-1069

1989

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Secretin pancreozymin stimulation test and confirmation of the diagnosis of cystic fibrosis

Gut, 1982-09, Vol.23 (9), p.744-750

1982

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Guanosine triphosphate cyclohydrolase I deficiency: early diagnosis by routine urine pteridine screening

Pediatrics (Evanston), 1987-03, Vol.79 (3), p.374-378

1987

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Use of a dried blood spot in immunoreactive-trypsin assay for detection of cystic fibrosis in infants

Clinical chemistry (Baltimore, Md.), 1981-05, Vol.27 (5), p.678-680

1981

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Detection of cystic fibrosis protein by electrofocusing

Pediatric research, 1978-07, Vol.12 (7), p.800-800

1978

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Comparison of the carbohydrate composition of alpha 2-macroglobulin from patients with cystic fibrosis and normal controls

Pediatric research, 1985-04, Vol.19 (4), p.344-346

1985

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Isolation of pure, active α 2 macroglobulin from small-scale plasma samples

Clinica chimica acta, 1982-01, Vol.118 (1), p.21-31

1982

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Protease binding by α 2 macroglobulin in cystic fibrosis

Clinica chimica acta, 1982-01, Vol.118 (1), p.33-43

1982

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Diagnosing cystic fibrosis in adults

The New England journal of medicine, 1979-05, Vol.300 (20), p.1164-1164

1979

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Conclusions from a pilot immunoreactive trypsin newborn screen for cystic fibrosis

Clinical chemistry (Baltimore, Md.), 1983-08, Vol.29 (8), p.1559-1560

1983

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Infection with Burkholderia cepacia Complex Genomovars in Patients with Cystic Fibrosis: Virulent Transmissible Strains of Genomovar III Can Replace Burkholderia multivorans

Epidemiology of Pseudomonas aeruginosa in Cystic Fibrosis in British Columbia, Canada

An unusual presentation of doxycycline-induced photosensitivity

Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy

Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiency

A genomic approach to mutation analysis of holocarboxylase synthetase gene in three Chinese patients with late-onset holocarboxylase synthetase deficiency

Treatment of recurrent hemoptysis in a child with cystic fibrosis by repeated bronchial artery embolizations and long-term tranexamic acid

Orthotopic liver transplantation in a patient with carbamyl phosphate synthetase deficiency and cystic fibrosis

Selective media for isolation of Burkholderia (Pseudomonas) cepacia from the respiratory secretions of patients with cystic fibrosis

Bone marrow transplantation in Gaucher's disease : effect of mixed chimeric state

Cardiomyopathy associated with nonendemic selenium deficiency in a Caucasian adolescent

Pseudomonas aeruginosa colonization of the gastrointestinal tract in patients with cystic fibrosis

Allelic association and linkage studies in Wilson disease

The high incidence of valproate hepatotoxicity in infants may relate to familial metabolic defects

Biochemical investigation of a child with molybdenum cofactor deficiency

Communicability of Pseudomonas infections in patients with cystic fibrosis

Secretin pancreozymin stimulation test and confirmation of the diagnosis of cystic fibrosis

Guanosine triphosphate cyclohydrolase I deficiency: early diagnosis by routine urine pteridine screening

Use of a dried blood spot in immunoreactive-trypsin assay for detection of cystic fibrosis in infants

Detection of cystic fibrosis protein by electrofocusing

Comparison of the carbohydrate composition of alpha 2-macroglobulin from patients with cystic fibrosis and normal controls

Isolation of pure, active α 2 macroglobulin from small-scale plasma samples

Protease binding by α 2 macroglobulin in cystic fibrosis

Diagnosing cystic fibrosis in adults

Conclusions from a pilot immunoreactive trypsin newborn screen for cystic fibrosis

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