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Clinical uses of intravenous immunoglobulin

Clinical and experimental immunology, 2005-10, Vol.142 (1), p.1-11

2005

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SLC3A1 and SLC7A9 Mutations in Autosomal Recessive or Dominant Canine Cystinuria: A New Classification System

Journal of veterinary internal medicine, 2013-11, Vol.27 (6), p.1400-1408

2013

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Do ribosomopathies explain some cases of common variable immunodeficiency

Clinical and experimental immunology, 2011-01, Vol.163 (1), p.96-103

2011

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Clinical Immunology Review Series: An approach to the use of the immunology laboratory in the diagnosis of clinical allergy

Clinical and experimental immunology, 2008-07, Vol.153 (1), p.10-18

2008

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Using calculated globulin fraction to reduce diagnostic delay in primary and secondary hypogammaglobulinaemias: results of a demonstration project

Annals of clinical biochemistry, 2015-05, Vol.52 (3), p.319-326

2015

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Transient renal Fanconi syndrome in a Chihuahua exposed to Chinese chicken jerky treats

Tierärztliche Praxis. Ausgabe K, Kleintiere/Heimtiere, 2015-01, Vol.43 (3), p.188

2015

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Suicide Attempt by Self-poisoning: Characteristics of Suicide Attempters Seen at the Emergency Room at the University Hospital of the West Indies

West Indian medical journal, 2012-08, Vol.61 (5), p.526-531

2012

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Depressive Symptoms in Adolescents in Jamaica

West Indian medical journal, 2012-08, Vol.61 (5), p.494-498

2012

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Ethylmalonic encephalopathy: clinical and biochemical observations

Neuropediatrics, 2007-04, Vol.38 (2), p.78

2007

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Deficiency in circulating natural killer (NK) cell subsets in common variable immunodeficiency and X‐linked agammaglobulinaemia

Clinical and experimental immunology, 2000-09, Vol.121 (3), p.506-514

2000

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British Association of Dermatologists guidelines for the management of people with chronic urticaria 2021

British journal of dermatology (1951), 2022-03, Vol.186 (3), p.398-413

2022

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Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency

Pediatric research, 2001, Vol.49 (1), p.18-23

2001

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Antibody deficiency

Journal of clinical pathology, 2008-09, Vol.61 (9), p.994-1000

2008

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Hyperinsulinaemic hypoglycaemia—Leading symptom in a patient with congenital disorder of glycosylation Ia (phosphomannomutase deficiency)

Journal of inherited metabolic disease, 2001-12, Vol.24 (8), p.858-862

2001

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Limited value of testing for intrinsic factor antibodies with negative gastric parietal cell antibodies in pernicious anaemia

Journal of clinical pathology, 2009-05, Vol.62 (5), p.439-441

2009

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4,5‐Dimethyl‐3‐hydroxy‐2[5H]‐furanone (sotolone) — The odour of maple syrup urine disease

Journal of inherited metabolic disease, 1999-04, Vol.22 (2), p.107-114

1999

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Polycystic kidneys and GM2 gangliosidosis-like disease in neonatal springboks (Antidorcas marsupialis)

Veterinary pathology, 2015-05, Vol.52 (3), p.543

2015

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The value of total IgE levels in the context of specific allergy

Pediatric allergy and immunology, 2008-12, Vol.19 (8), p.777-778

2008

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Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short‐chain acyl‐CoA dehydrogenase gene

Journal of inherited metabolic disease, 2003-07, Vol.26 (1), p.37-42

2003

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Some cases of common variable immunodeficiency may be due to a mutation in the SBDS gene of Shwachman-Diamond syndrome

Clinical and experimental immunology, 2008-03, Vol.151 (3), p.448-454

2008

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The effect of carnitine supplementation in valproate-induced hyperammonaemia

Acta Paediatrica, 1996-04, Vol.85 (4), p.446-449

1996

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Evaluation of serum cobalamin concentration in cats with clinical signs of gastrointestinal disease

Schweizer Archiv für Tierheilkunde, 2012-11, Vol.154 (11), p.479-486

2012

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False Diagnosis of Maple Syrup Urine Disease Owing to Ingestion of Herbal Tea

The New England journal of medicine, 1999-09, Vol.341 (10), p.769-769

1999

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Cystinuria in a girl presenting with a hyperechogenic colon detected by prenatal ultrasonography and a new SLC3A1 gene mutation (p.Phe278Ser)

Ultraschall in der Medizin, 2014-10, Vol.35 (5), p.473

2014

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Clinical uses of intravenous immunoglobulin

SLC3A1 and SLC7A9 Mutations in Autosomal Recessive or Dominant Canine Cystinuria: A New Classification System

Do ribosomopathies explain some cases of common variable immunodeficiency

Clinical Immunology Review Series: An approach to the use of the immunology laboratory in the diagnosis of clinical allergy

Using calculated globulin fraction to reduce diagnostic delay in primary and secondary hypogammaglobulinaemias: results of a demonstration project

Transient renal Fanconi syndrome in a Chihuahua exposed to Chinese chicken jerky treats

Suicide Attempt by Self-poisoning: Characteristics of Suicide Attempters Seen at the Emergency Room at the University Hospital of the West Indies

Depressive Symptoms in Adolescents in Jamaica

Ethylmalonic encephalopathy: clinical and biochemical observations

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

Deficiency in circulating natural killer (NK) cell subsets in common variable immunodeficiency and X‐linked agammaglobulinaemia

British Association of Dermatologists guidelines for the management of people with chronic urticaria 2021

Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency

Antibody deficiency

Hyperinsulinaemic hypoglycaemia—Leading symptom in a patient with congenital disorder of glycosylation Ia (phosphomannomutase deficiency)

Limited value of testing for intrinsic factor antibodies with negative gastric parietal cell antibodies in pernicious anaemia

4,5‐Dimethyl‐3‐hydroxy‐2[5H]‐furanone (sotolone) — The odour of maple syrup urine disease

Polycystic kidneys and GM2 gangliosidosis-like disease in neonatal springboks (Antidorcas marsupialis)

The value of total IgE levels in the context of specific allergy

Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short‐chain acyl‐CoA dehydrogenase gene

Some cases of common variable immunodeficiency may be due to a mutation in the SBDS gene of Shwachman-Diamond syndrome

The effect of carnitine supplementation in valproate-induced hyperammonaemia

Evaluation of serum cobalamin concentration in cats with clinical signs of gastrointestinal disease

False Diagnosis of Maple Syrup Urine Disease Owing to Ingestion of Herbal Tea

Cystinuria in a girl presenting with a hyperechogenic colon detected by prenatal ultrasonography and a new SLC3A1 gene mutation (p.Phe278Ser)

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