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A Erikson

Showing results (11-20 of 48) with videos related to

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Journal of Speech, Language, and Hearing Research : JSLHR|June 18, 2020
The Relationship Between Word Learning and Executive Function in Preschoolers With and Without Developmental Language DisorderLeah L Kapa, Jessie A Erikson
Clinical Genetics|December 1, 1989
Hereditary spastic diplegia with mental retardation in two young siblingsK H Gustavson, K Modrzewska, A Erikson
Neuropediatrics|August 1, 1995
Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher diseaseA Erikson, M Aström, J E Månsson
American Journal of Human Genetics|August 1, 1990
Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase geneN Dahl, M Lagerström, A Erikson, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 1, 1995
Outcome of pregnancy in women with myotonic dystrophy and analysis of CTG gene expansionA Erikson, H Forsberg, U Drugge, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 13, 2003
Free sialic acid storage (Salla) disease in SwedenA Erikson, N Aula, P Aula, et al.
BMC Bioinformatics|August 10, 2018
BART: bioinformatics array research toolMaria Luisa Amaral, Galina A Erikson, Maxim N Shokhirev
Pediatric Neurology|March 1, 1987
Gaucher disease (type III): intellectual profileA Erikson, J Karlberg, A L Skogman, et al.
Neuropediatrics|August 1, 1993
Enzyme replacement therapy of infantile Gaucher diseaseA Erikson, K Johansson, J E Månsson, et al.
Genomics|November 1, 1988
Tight linkage between type III Gaucher's disease (Norrbottnian type) and a MspI polymorphism within the gene for human glucocerebrosidaseN Dahl, A Erikson, K Hammarström-Heeroma, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Journal of Speech, Language, and Hearing Research : JSLHR|June 18, 2020
The Relationship Between Word Learning and Executive Function in Preschoolers With and Without Developmental Language DisorderLeah L Kapa, Jessie A Erikson
Clinical Genetics|December 1, 1989
Hereditary spastic diplegia with mental retardation in two young siblingsK H Gustavson, K Modrzewska, A Erikson
Neuropediatrics|August 1, 1995
Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher diseaseA Erikson, M Aström, J E Månsson
American Journal of Human Genetics|August 1, 1990
Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase geneN Dahl, M Lagerström, A Erikson, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 1, 1995
Outcome of pregnancy in women with myotonic dystrophy and analysis of CTG gene expansionA Erikson, H Forsberg, U Drugge, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 13, 2003
Free sialic acid storage (Salla) disease in SwedenA Erikson, N Aula, P Aula, et al.
BMC Bioinformatics|August 10, 2018
BART: bioinformatics array research toolMaria Luisa Amaral, Galina A Erikson, Maxim N Shokhirev
Pediatric Neurology|March 1, 1987
Gaucher disease (type III): intellectual profileA Erikson, J Karlberg, A L Skogman, et al.
Neuropediatrics|August 1, 1993
Enzyme replacement therapy of infantile Gaucher diseaseA Erikson, K Johansson, J E Månsson, et al.
Genomics|November 1, 1988
Tight linkage between type III Gaucher's disease (Norrbottnian type) and a MspI polymorphism within the gene for human glucocerebrosidaseN Dahl, A Erikson, K Hammarström-Heeroma, et al.
Pageof 5