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Olaf A Bodamer

Showing results (1-10 of 65) with videos related to

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Clinical Therapeutics|April 9, 2008
Newborn screening in Fabry disease: what can be achieved with early diagnosis?Olaf A Bodamer
Wiener Medizinische Wochenschrift (1946)|August 18, 2010
Laboratory and genetic evaluation of Gaucher diseaseOlaf A Bodamer, Christina Hung
Current Protocols in Human Genetics|October 18, 2012
Diagnosing lysosomal storage disorders: Pompe diseaseOlaf A Bodamer, Angela Dajnoki
European Journal of Clinical Investigation|June 18, 2004
Fabry disease definedC Stromberger, Olaf A Bodamer
Journal of Child Neurology|August 2, 2002
Practical management of combined methylmalonicaciduria and homocystinuriaDebra L Smith, Olaf A Bodamer
American Journal of Medical Genetics. Part A|June 9, 2005
Central nervous system malformations in oral-facial-digital syndrome, type 1Margareta Holub, Lorraine Potocki, Olaf A Bodamer
Molecular Genetics and Metabolism|August 17, 2014
The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscapeOlaf A Bodamer, Roberto Giugliani, Tim Wood
Journal of Pediatric Genetics|February 10, 2017
Newborn Screening for Lysosomal Storage DisordersRoy W A Peake, Olaf A Bodamer
Current Protocols in Human Genetics|April 19, 2013
Diagnosing lysosomal storage disorders: Fabry diseaseOlaf A Bodamer, Britt Johnson, Angela Dajnoki
Clinical Chemistry|March 1, 2017
Dark Colored Urine in a 2-Year-Old ChildRoy W A Peake, Olaf A Bodamer
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Clinical Therapeutics|April 9, 2008
Newborn screening in Fabry disease: what can be achieved with early diagnosis?Olaf A Bodamer
Wiener Medizinische Wochenschrift (1946)|August 18, 2010
Laboratory and genetic evaluation of Gaucher diseaseOlaf A Bodamer, Christina Hung
Current Protocols in Human Genetics|October 18, 2012
Diagnosing lysosomal storage disorders: Pompe diseaseOlaf A Bodamer, Angela Dajnoki
European Journal of Clinical Investigation|June 18, 2004
Fabry disease definedC Stromberger, Olaf A Bodamer
Journal of Child Neurology|August 2, 2002
Practical management of combined methylmalonicaciduria and homocystinuriaDebra L Smith, Olaf A Bodamer
American Journal of Medical Genetics. Part A|June 9, 2005
Central nervous system malformations in oral-facial-digital syndrome, type 1Margareta Holub, Lorraine Potocki, Olaf A Bodamer
Molecular Genetics and Metabolism|August 17, 2014
The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscapeOlaf A Bodamer, Roberto Giugliani, Tim Wood
Journal of Pediatric Genetics|February 10, 2017
Newborn Screening for Lysosomal Storage DisordersRoy W A Peake, Olaf A Bodamer
Current Protocols in Human Genetics|April 19, 2013
Diagnosing lysosomal storage disorders: Fabry diseaseOlaf A Bodamer, Britt Johnson, Angela Dajnoki
Clinical Chemistry|March 1, 2017
Dark Colored Urine in a 2-Year-Old ChildRoy W A Peake, Olaf A Bodamer
Pageof 7