A. Davidson

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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.

P. Vandamme, E. Mahenthiralingam, D. Speert, 2001, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Evidence for calcitonin--a new hormone from the parathyroid that lowers blood calcium.

D. Copp, A. Davidson, E. Cameron, 1962, Endocrinology.

S. J. James, S. Innis, A. Davidson, 2007, The American journal of clinical nutrition.

Phosphatidylcholine and lysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S-adenosylhomocysteine, and S-adenosylmethionine.

S. J. James, S. Innis, A. Davidson, 2005, The American journal of clinical nutrition.

Epstein-Barr virus shedding in breast milk.

R. B. Forsyth, A. Junker, L. Rymo, 1991, The American journal of the medical sciences.

Pasteurization Efficiency of a HTST System for Human Milk

S. Nakai, B. Skura, J. Dhar, 1996 .

Letter to the Editor: Detection of Cystic Fibrosis Protein by Electrofocusing

D. Applegarth, L. Wong, A. Davidson, 1978, Pediatric Research.

Renal function in pediatric cystic fibrosis patients in the first decade of life

M. Chilvers, C. White, A. Davidson, 2011, Pediatric Nephrology.

Role of exercise and nutrition status on bone mineral density in cystic fibrosis.

P. Paré, J. Raboud, D. Kendler, 2003, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Isolation of pure, active α2 macroglobulin from small-scale plasma samples

D. Applegarth, L. Wong, A. Davidson, 1982 .

Epidemiology of Pseudomonas aeruginosa in cystic fibrosis in British Columbia, Canada.

E. Mahenthiralingam, D. Speert, M. Campbell, 2002, American journal of respiratory and critical care medicine.

Plasma choline depletion is associated with decreased peripheral blood leukocyte acetylcholine in children with cystic fibrosis.

S. Innis, D. Hasman, A. Davidson, 2011, The American journal of clinical nutrition.

Case report: diagnosis and management of type I hyperlipoproteinemia.

S. Israels, D. Applegarth, A. Davidson, 1975, Journal of the American Dietetic Association.

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

L. Wong, A. Davidson, Y.P. Liliquist, 1996, Pediatric pulmonology.

α1-Antitrypsin Deficiency Alleles in Cystic Fibrosis Lung Disease

M. Corey, J. Zieleński, A. Freitag, 2003 .

Long-term comparative trial of positive expiratory pressure versus oscillating positive expiratory pressure (flutter) physiotherapy in the treatment of cystic fibrosis.

L. Wong, A. Davidson, P. Mcilwaine, 2001, The Journal of pediatrics.

Long-term comparative trial of conventional postural drainage and percussion versus positive expiratory pressure physiotherapy in the treatment of cystic fibrosis.

L. Wong, A. Davidson, P. Mcilwaine, 1997, The Journal of pediatrics.

Muscular performance in cystic fibrosis patients and its relation to vitamin E.

I. D. Desai, A. Davidson, C. Darby, 1973, Archives of disease in childhood.

Mucoid and nonmucoid Burkholderia cepacia complex bacteria in cystic fibrosis infections.

R. Brant, D. Speert, P. Wilcox, 2011, American journal of respiratory and critical care medicine.

Immunoreactive trypsin in cystic fibrosis.

D. Applegarth, L. Wong, A. Davidson, 1984, Journal of pediatric gastroenterology and nutrition.

Economic effects of an eradication protocol for first appearance of Pseudomonas aeruginosa in cystic fibrosis patients: 1995 vs. 2009.

A. Davidson, E. Cho, Y. Lillquist, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Delays in diagnosing cystic fibrosis: can we find ways to diagnose it earlier?

H. Vallance, A. Davidson, M. Steinraths, 2008, Canadian family physician Medecin de famille canadien.

Monitoring of serum prolactin in pediatric patients with cystic fibrosis who are receiving domperidone.

A. Davidson, E. Cho, Patricia Gerber, 2009, The Canadian journal of hospital pharmacy.

Cystic fibrosis: the effect of medium from cultured cystic fibrosis fibroblasts on ATPase activity.

B. Roufogalis, D. Applegarth, A. Davidson, 1977, Clinica chimica acta; international journal of clinical chemistry.

Direct Humoral Control of Parathyroid Function in the Dog.∗ †

D. Copp, A. Davidson, 1961, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Evaluation of a multidimensional cystic fibrosis transition program: a quality improvement initiative.

M. Chilvers, A. Gravelle, A. Davidson, 2015, Journal of pediatric nursing.

The Synacthen Test of Adrenal Cortical Function in Children

C. Johnston, A. Davidson, C. Johnston, 1968, Clinical pediatrics.

CARCINOEMBRYONIC ANTIGEN IN CYSTIC FIBROSIS

A. Davidson, Wilcox Me, E. K. Mincey, 1973 .

An Unusual Presentation of Doxycycline-Induced Photosensitivity

L. Wong, A. Davidson, J. Prendiville, 2000, Pediatrics.

Increased plasma homocysteine and S-adenosylhomocysteine and decreased methionine is associated with altered phosphatidylcholine and phosphatidylethanolamine in cystic fibrosis.

S. J. James, R. Dyer, S. Innis, 2003, The Journal of pediatrics.

Review of Metabolic Screening Program of Children's Hospital, Vancouver, British Columbia. 1971--1977.

D. Hardwick, D. Applegarth, L. Wong, 1979, Clinical biochemistry.

Burkholderia cepacia in cystic fibrosis. Variable disease course.

J. Raboud, E. Mahenthiralingam, P. Wilcox, 1999, American journal of respiratory and critical care medicine.

Oral zinc therapy in the treatment of α-mannosidosis

H. Vallance, A. Savage, D. Applegarth, 1993 .

Barrett's esophagus in children with cystic fibrosis: not a coincidental association.

E. Hassall, D. Israel, L. Wong, 1993, The American journal of gastroenterology.

Effects of a Pseudomonas aeruginosa eradication policy in a cystic fibrosis clinic

M. Chilvers, A. Davidson, Y. Lillquist, 2012, Current opinion in pulmonary medicine.

Communicability of Pseudomonas infections in patients with cystic fibrosis.

W. Paranchych, D. Speert, L. Wong, 1989, The Journal of pediatrics.

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

N. Cimolai, L. Wong, A. Davidson, 1995, Journal of clinical pathology.

References Subscriptions Permissions Email Alerts Innate Immunity Mediated by TLR5 as a Novel Antiinflammatory Target for Cystic

R. Hancock, Kelly D. Smith, S. Turvey, 2013 .

The High Incidence of Valproate Hepatotoxicity in Infants May Relate to Familial Metabolic Defects

J. Dimmick, D. Applegarth, A. Davidson, 1990, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Protease binding by α2 macroglobulin in cystic fibrosis

D. Applegarth, L. Wong, A. Davidson, 1982 .

Argininosuccinic aciduria A developmental and biochemical case study

D. Applegarth, J. Toone, J. Crichton, 1983, Journal of the Neurological Sciences.

The relation of cerebrospinal fluid and plasma glycine levels in propionic acidaemia, a ‘ketotic hyperglycinaemia’

J. Sass, S. Korman, D. Karall, 2008, Journal of Inherited Metabolic Disease.

Cystic fibrosis and control nasal epithelial cells harvested by a brushing procedure

A. Davidson, M. Bridges, D. C. Walker, 1991, In Vitro Cellular & Developmental Biology – Animal.

Celiac Disease and Dermatitis Herpetiformis: National survey indicates delays in diagnosis.

J. Campbell, A. Davidson, 1992, Canadian family physician Medecin de famille canadien.

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

D. Speert, M. Campbell, L. Wong, 1993, The Journal of infectious diseases.

Cardiomyopathy associated with nonendemic selenium deficiency in a Caucasian adolescent.

G. Lockitch, L. Wong, A. Davidson, 1990, The American journal of clinical nutrition.

Alpha 1-antitrypsin deficiency alleles in cystic fibrosis lung disease.

M. Corey, J. Zieleński, A. Freitag, 2003, American journal of respiratory cell and molecular biology.

Cystic fibrosis and nutrition: linking phospholipids and essential fatty acids with thiol metabolism.

S. Innis, A. Davidson, S. M. Innis, 2008, Annual review of nutrition.

Reducing substances in neonatal stools detected by Clinitest.

A. Davidson, M. Mullinger, 1970, Pediatrics.

Biochemical and Histologic Pathology in an Infant with Cross-Reacting Material (Negative) Pyruvate Carboxylase Deficiency

G. Pirie, M. Norman, J. Dimmick, 1986, Pediatric Research.

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

D. Hardwick, D. Applegarth, L. Wong, 1981, Clinical chemistry.

Plasma arginine esterase activity in cystic fibrosis of the pancreas.

D. Applegarth, A. Davidson, A. George, 1977, Clinica chimica acta; international journal of clinical chemistry.

Use of a DriedBloodSpot in Immunoreactive-TrypsinAssayfor Detection of CysticFibrosisin Infants

D. Hardwick, D. Applegarth, L. Wong, 2004 .

Useofa DriedBloodSpotinImmunoreactive-Trypsin AssayforDetection of CysticFibrosis inInfants

D. Hardwick, D. Applegarth, L. Wong, 1981 .

Anti-plasmin (α2-macroglobulin) activity of plasma from cystic fibrosis patients

D. Applegarth, L. Wong, A. Davidson, 1978 .

Biochemical investigation of a child with molybdenum cofactor deficiency.

G. Lockitch, J. Johnson, D. Applegarth, 1990, Clinical biochemistry.

Airway clearance techniques in the treatment of cystic fibrosis.

A. Davidson, M. McIlwaine, Davidson Ag, 1996, Current opinion in pulmonary medicine.

Newborn screening for MCAD deficiency: experience of the first three years in British Columbia, Canada.

B. Andresen, P. Waters, G. Horvath, 2008, Canadian journal of public health = Revue canadienne de sante publique.

Newborn Screening for MCAD Deficiency

B. Andresen, P. Waters, G. Horvath, 2008 .

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

L. Wong, A. Davidson, S. Turtle, 1982, Gut.

Phthalate metabolites in urine of CF patients are associated with use of enteric-coated pancreatic enzymes.

S. Innis, B. Keller, A. Davidson, 2009, Environmental toxicology and pharmacology.

Conclusions from a pilot immunoreactive trypsin newborn screen for cystic fibrosis.

D. Hardwick, D. Applegarth, L. Wong, 1983, Clinical Chemistry.

Screening for celiac disease.

E. Hassall, A. Davidson, 1997, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

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

E. Naylor, D. Applegarth, L. Wong, 1987, Pediatrics.

Effects of ultrasonic homogenization of human milk on lipolysis, IgA, IgG, lactoferrin and bacterial content

J. Anderson, I. Desai, F. Martinez, 1992 .

Ultrasonic homogenization of expressed human milk to prevent fat loss during tube feeding.

I. Desai, F. Martinez, A. Davidson, 1987, Journal of pediatric gastroenterology and nutrition.

Ultrasonication, Lyophilization, Freezing and Storage Effects on Fat Loss during Mechanical Infusion of Expressed Human Milk

S. Nakai, I. Desai, J. Dhar, 1995 .

Oral zinc therapy in the treatment of alpha-mannosidosis.

H. Vallance, A. Savage, D. Applegarth, 1993, American journal of medical genetics.

Choiceof a SatisfactoryEvacuated Blood-CollectionTubefor Magnesiumand Zinc Assays

D. Hardwick, D. Applegarth, L. Wong, 2004 .