A. Erikson

发表

Outcome of pregnancy in women with myotonic dystrophy and analysis of CTG gene expansion

G. Holmgren, U. Drugge, H. Forsberg, 1995, Acta paediatrica.

Early onset autosomal dominant spinocerebellar ataxia with miosis: four cases.

U. Eriksson, E. Stattin, A. Erikson, 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients.

P. Kaplan, J. Charrow, H. Andersson, 2004, Seminars in hematology.

Gaucher disease-norrbottnian type

B. Hagberg, S. Dreborg, A. Erikson, 1980, European Journal of Pediatrics.

Management of neuronopathic Gaucher disease: Revised recommendations

R. Schiffmann, B. Bembi, A. Tylki-Szymańska, 2009, Journal of Inherited Metabolic Disease.

5 Neuronopathic forms of Gaucher's disease

R. Schiffmann, B. Bembi, A. Erikson, 1997 .

Ten years' experience of bone marrow transplantation for Gaucher disease.

O. Ringdén, J. Månsson, C. Groth, 1995, Transplantation.

Enzyme Replacement Therapy of Infantile Gaucher Disease

J. Månsson, L. Svennerholm, A. Erikson, 1993, Neuropediatrics.

Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase gene.

U. Pettersson, N. Dahl, M. Lagerström, 1990, American journal of human genetics.

Gaucher disease (type III): intellectual profile.

S. Dreborg, A. Erikson, J. Karlberg, 1987, Pediatric neurology.

Free sialic acid storage (Salla) disease in Sweden

J. Månsson, N. Aula, P. Aula, 2002, Acta paediatrica.

Neuropathology of the Norrbottnian type of Gaucher disease

N. Conradi, L. Svennerholm, P. Sourander, 1984, Acta Neuropathologica.

Characteristics of primary biliary cirrhosis in British Columbia's First Nations population.

L. Arbour, E. Yoshida, R. Rupps, 2005, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

Gaucher disease — Norrbottnian type Ocular abnormalities

A. Erikson, I. Wahlberg, 1985, Acta ophthalmologica.

Outcome of type III Gaucher disease on enzyme replacement therapy: Review of 55 cases

A. Tylki-Szymańska, A. Vellodi, E. Mengel, 2007, Journal of Inherited Metabolic Disease.

Ten years' experience of enzyme infusion therapy of Norrbottnian (type 3) Gaucher disease.

J. Månsson, Magnus Nilsson, H. Forsberg, 2006, Acta paediatrica.

Management of neuronopathic Gaucher disease: A European consensus

B. Bembi, A. Rolfs, A. Tylki-Szymańska, 2001, Journal of Inherited Metabolic Disease.

The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: A position statement

G. Andria, J. M. Aerts, B. Bembi, 2003, Journal of Inherited Metabolic Disease.

Ten years’ experience of enzyme infusion therapy of Norrbottnian (type 3) Gaucher disease

J. Månsson, Magnus Nilsson, H. Forsberg, 2006 .

Remaining problems in the management of patients with Gaucher disease

A. Erikson, 2001, Journal of Inherited Metabolic Disease.

Neuronopathic forms of Gaucher's disease.

R. Schiffmann, B. Bembi, A. Erikson, 1997, Bailliere's clinical haematology.

Gaucher disease‐Norrbottnian type (III)

A. Erikson, 1986, Acta paediatrica Scandinavica. Supplement.

Gaucher disease. Current issues in diagnosis and treatment. NIH Technology Assessment Panel on Gaucher Disease.

W. H. Hall, Robin E Berman, F. Collins, 1996, JAMA.

LONG‐TERM FOLLOW‐UP OF THE FIRST SUCCESSFUL BONE MARROW TRANSPLANTATION IN GAUCHER DISEASE

L. Svennerholm, C. Groth, S. Granqvist, 1988, Transplantation.

Glycerol kinase deficiency: follow‐up during 20 years, genetics, biochemistry and prognosis

S. Lindstedt, G. Samuelson, A. Erikson, 2004, Acta paediatrica.

There Are Two Different Species B Adenovirus Receptors: sBAR, Common to Species B1 and B2 Adenoviruses, and sB2AR, Exclusively Used by Species B2 Adenoviruses

A. Segerman, G. Wadell, N. Arnberg, 2003, Journal of Virology.

Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15.

L. Peltonen, J. Weissenbach, J. Schleutker, 1995, American journal of human genetics.

Simplified detection of Nci mutation in Gaucher disease

U. Pettersson, N. Dahl, A. Erikson, 1990, The Lancet.

Tight linkage between type III Gaucher's disease (Norrbottnian type) and a MspI polymorphism within the gene for human glucocerebrosidase.

U. Pettersson, N. Dahl, A. Erikson, 1988, Genomics.

Clinical and Biochemical Outcome of Marrow Transplantation for Gaucher Disease of the Norrbottnian Type

O. Ringdén, J. Månsson, L. Svennerholm, 1990, Acta paediatrica Scandinavica.

Gaucher disease—Norrbottnian type

S. Blom, A. Erikson, 1983, European Journal of Pediatrics.

Neurodevelopmental, neurological, and neurophysiological aspects

S. Blom, A. Erikson, 1983 .

Hereditary spastic diplegia with mental retardation in two young siblings

K. Gustavson, A. Erikson, K. Modrzewska, 1989, Clinical genetics.

New type of spinocerebellar degeneration syndrome in a northern Swedish population

K. Gustavson, A. Erikson, K. Modrzewska, 1987, Clinical Genetics.

Gaucher disease of the Norrbottnian type (type III). Phenotypic manifestations.

L. Svennerholm, C. Groth, S. Dreborg, 1982, Progress in clinical and biological research.

Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher disease.

J. Månsson, A. Erikson, M. Åström, 1995, Neuropediatrics.

HEREDITARY SYNDROME CONSISTING IN RECURRENT ATTACKS RESEMBLING BRACHIAL PLEXUS NEURITIS, SPECIAL FACIAL FEATURES, AND CLEFT PALATE

A. Erikson, 1974, Acta paediatrica Scandinavica.

The mystery of primary biliary cirrhosis in British Columbia’s First Nations people

L. Arbour, E. Yoshida, A. Erikson, 2004, International journal of circumpolar health.

Ataxia, autism, and the cerebellum: a clinical study of 32 individuals with congenital ataxia

C. Gillberg, O. Flodmark, A. Erikson, 2005, Developmental medicine and child neurology.

Norrbottnian type of Gaucher disease--clinical, biochemical and molecular biology aspects: successful treatment with bone marrow transplantation.

O. Ringdén, J. Månsson, L. Svennerholm, 1991, Developmental neuroscience.

Gaucher disease: Current issues in diagnosis and treatment

W. H. Hall, Robin E Berman, F. Collins, 1996 .

Hematological findings in the Norrbottnian type of Gaucher disease

L. Svennerholm, S. Dreborg, A. Erikson, 1982, European Journal of Pediatrics.