M. Bain

发表

In vitro and in vivo studies with human carrier erythrocytes loaded with polyethylene glycol‐conjugated and native adenosine deaminase

B. Bax, R. Chalmers, L. Fairbanks, 2000, British journal of haematology.

Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children

J. Zschocke, R. Chalmers, H. Michelakakis, 2006, Journal of Inherited Metabolic Disease.

Ca2+ channels in human term trophoblast cells in vitro. A study using the Ca2+-sensitive dye fura 2

M. Zaidi, B. Bax, M. Bain, 1994 .

The entrapment of polyethylene glycol-bound adenosine deaminase (Pegademase) in human carrier erythrocytes.

H. Simmonds, B. Bax, R. Chalmers, 1996, Biochemical Society transactions.

The mouse immune response to carrier erythrocyte entrapped antigens.

A. M. Murray, B. Bax, R. Chalmers, 2006, Vaccine.

Survival of human carrier erythrocytes in vivo.

B. Bax, R. Chalmers, M. Bain, 1999, Clinical science.

In Vivo Survival of Human Energy-Replete Carrier Erythrocytes

B. Bax, R. Chalmers, M. Bain, 1997 .

The Entrapment of Polyethylene Glycol-Conjugated Adenosine Deaminase (Pegademase) and Native Adenosine Deaminase in Human Carrier Erythrocytes

H. Simmonds, B. Bax, R. Chalmers, 1997 .

Carrier erythrocyte entrapped adenosine deaminase therapy in adenosine deaminase deficiency.

H. Simmonds, B. Bax, R. Chalmers, 2000, Advances in Experimental Medicine and Biology.

THERAPY FOR MNGIE CARRIER ERYTHROCYTE ENTRAPPED THYMIDINE PHOSPHORYLASE

B. Bax, N. Moran, M. Bain, 2008 .

Erythrocyte Encapsulated Thymidine Phosphorylase for the Treatment of Patients with Mitochondrial Neurogastrointestinal Encephalomyopathy: Study Protocol for a Multi-Centre, Multiple Dose, Open Label Trial

H. Mandel, P. Sedgwick, S. Rahman, 2019, Journal of clinical medicine.

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism.

G. Addison, P. Littlejohns, J. Lord, 1998, Journal of public health medicine.

Isolated congenital ACTH deficiency: a cleavage enzyme defect?

M. Bain, A. Johnstone, S. Nussey, 1994, Clinical endocrinology.

CONTRIBUTION OF GUT BACTERIAL METABOLISM TO HUMAN METABOLIC DISEASE

T. E. Stacey, R. Chalmers, M. Bain, 1988, The Lancet.

Use of human somatotrophin in the treatment of a patient with methylmalonic aciduria

S. Nussey, R. Chalmers, M. Bain, 1995, European Journal of Pediatrics.

Simultaneous Occurrence of Mucopolysaccharide Type Ii Disease (Hunter's Syndrome) and Systemic Lupus Erythematosus in a Paediatric Patient

M. Bain, A. Russell, R. Periera, 1992, Journal of the Royal Society of Medicine.

Newborn screening for inborn errors of metabolism: a systematic review.

A. Culyer, P. Bower, G. Addison, 1997, Health technology assessment.

Oral cobalamin therapy

R. Chalmers, M. Bain, lan Costello, 2000, The Lancet.

Hair loss in children.

R. Chalmers, M. Bain, 1993, Archives of disease in childhood.

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

M. Pourfarzam, J. Zschocke, S. Kölker, 2003, Neuropediatrics.

Enzymologic Studies on Patients with Methylmalonic Aciduria: Basis for a Clinical Trial of Deoxyadenosylcobalamin in a Hydroxocobalamin-Unresponsive Patient

R. Chalmers, M. Bain, J. Mistry, 1991, Pediatric Research.

Permeability of the human placenta in vivo to four non‐metabolized hydrophilic molecules.

A. Taylor, T. E. Stacey, M. Bain, 1990, The Journal of physiology.

Passive permeability of the human placenta 'in-vivo'

M. Bain, 1992 .

Unexplained gastrointestinal symptoms: think mitochondrial disease.

S. Travis, J. Poulton, B. Bax, 2014, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Clinical/Scientific Notes

P. Tonin, M. Filosto, B. Bax, 2011, Neurology.

A 9‐yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult‐type ADA deficiency

P. Ind, B. Bax, R. Chalmers, 2007, European journal of haematology.

Recalcitrant palmoplantar warts associated with adult‐onset adenosine deaminase deficiency

C. Harland, M. Bain, F. Antony, 2002, The British journal of dermatology.

Safety and Efficacy of Erythrocyte Encapsulated Thymidine Phosphorylase in Mitochondrial Neurogastrointestinal Encephalomyopathy

H. Mandel, M. Filosto, J. Poulton, 2019, Journal of clinical medicine.

Secondary analysis of economic data: a review of cost-benefit studies of neonatal screening for phenylketonuria.

G. Addison, P. Littlejohns, J. Lord, 1999, Journal of epidemiology and community health.

Riboflavin-responsive glutaryl CoA dehydrogenase deficiency.

J. Zschocke, R. Chalmers, M. Bain, 2006, Molecular genetics and metabolism.

In vivo permeability of the human placenta to inulin and mannitol.

T. E. Stacey, T E Stacey, M D Bain, 1988, The Journal of physiology.

CARRIER ERYTHROCYTE ENTRAPPED THYMIDINE PHOSPHORYLASE THERAPY FOR MNGIE

M. Muqit, B. Bax, N F Moran, 2008, Neurology.

Haemorheology in Gaucher disease

B. Bax, R. Chalmers, M. Rampling, 2005, European journal of haematology.