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Loren Pena

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American Journal of Medical Genetics. Part A|January 29, 2011
Fanconi-Bickel syndrome: report of life history and successful pregnancy in an affected patientLoren Pena, Joel Charrow
American Journal of Medical Genetics. Part A|June 9, 2012
Survey of health status and complications among propionic acidemia patientsLoren Pena, Barbara K Burton
Neuromuscular Disorders : NMD|April 2, 2010
Episodic myoglobinuria in a primary gamma-sarcoglycanopathyLoren Pena, Katherine Kim, Joel Charrow
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
Follow-up of patients with short-chain acyl-CoA dehydrogenase and isobutyryl-CoA dehydrogenase deficiencies identified through newborn screening: one center's experienceLoren Pena, Brad Angle, Barbara Burton, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Recurrent Anion Gap Acidosis: An Unusual Presentation of X-Linked Adrenoleukodystrophy in a Five-year-old MaleJoel Schwab, Loren Pena, Laura Sigman, et al.
Clinical Pediatrics|July 16, 2008
Two Children with macrocephaly, developmental delay, and PTEN mutationJoel G Schwab, Loren Pena, Darrel Waggoner, et al.
PM & R : the Journal of Injury, Function, and Rehabilitation|August 23, 2024
Why genetic testing is important in patients with developmental disabilities-a unique case of progressive hypertonia and chorea: VARS2-related disorderShannon Strader, Marissa Vawter-Lee, Loren Pena, et al.
American Journal of Medical Genetics. Part A|March 24, 2021
A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature reviewXiaolin Hu, Sofia Saenz Ayala, Lisa Dyer, et al.
Journal of Virology|August 7, 2002
Long-term effect of interferon on keratinocytes that maintain human papillomavirus type 31Yijan E Chang, Loren Pena, Ganes C Sen, et al.
Orphanet Journal of Rare Diseases|April 19, 2017
A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases NetworkRebecca C Spillmann, Allyn McConkie-Rosell, Loren Pena, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|January 29, 2011
Fanconi-Bickel syndrome: report of life history and successful pregnancy in an affected patientLoren Pena, Joel Charrow
American Journal of Medical Genetics. Part A|June 9, 2012
Survey of health status and complications among propionic acidemia patientsLoren Pena, Barbara K Burton
Neuromuscular Disorders : NMD|April 2, 2010
Episodic myoglobinuria in a primary gamma-sarcoglycanopathyLoren Pena, Katherine Kim, Joel Charrow
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
Follow-up of patients with short-chain acyl-CoA dehydrogenase and isobutyryl-CoA dehydrogenase deficiencies identified through newborn screening: one center's experienceLoren Pena, Brad Angle, Barbara Burton, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Recurrent Anion Gap Acidosis: An Unusual Presentation of X-Linked Adrenoleukodystrophy in a Five-year-old MaleJoel Schwab, Loren Pena, Laura Sigman, et al.
Clinical Pediatrics|July 16, 2008
Two Children with macrocephaly, developmental delay, and PTEN mutationJoel G Schwab, Loren Pena, Darrel Waggoner, et al.
PM & R : the Journal of Injury, Function, and Rehabilitation|August 23, 2024
Why genetic testing is important in patients with developmental disabilities-a unique case of progressive hypertonia and chorea: VARS2-related disorderShannon Strader, Marissa Vawter-Lee, Loren Pena, et al.
American Journal of Medical Genetics. Part A|March 24, 2021
A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature reviewXiaolin Hu, Sofia Saenz Ayala, Lisa Dyer, et al.
Journal of Virology|August 7, 2002
Long-term effect of interferon on keratinocytes that maintain human papillomavirus type 31Yijan E Chang, Loren Pena, Ganes C Sen, et al.
Orphanet Journal of Rare Diseases|April 19, 2017
A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases NetworkRebecca C Spillmann, Allyn McConkie-Rosell, Loren Pena, et al.
Pageof 3