Melissa P Wasserstein

Melissa P Wasserstein

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Melissa P Wasserstein

Melissa P Wasserstein

Publications by authors named "Melissa P Wasserstein"

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37Publications

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Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.

Am J Hum Genet 2019 Sep 22;105(3):493-508. Epub 2019 Aug 22.

Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, 00146 Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.07.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731364PMC
September 2019

Olipudase alfa for treatment of acid sphingomyelinase deficiency (ASMD): safety and efficacy in adults treated for 30 months.

J Inherit Metab Dis 2018 09 5;41(5):829-838. Epub 2018 Jan 5.

Clinical Development, Rare Diseases, Sanofi Genzyme, 1, Avenue Pierre Brossolette, 91385, Chilly-Mazarin, France.

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http://dx.doi.org/10.1007/s10545-017-0123-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133173PMC
September 2018

Long-term safety and efficacy of pegvaliase for the treatment of phenylketonuria in adults: combined phase 2 outcomes through PAL-003 extension study.

Orphanet J Rare Dis 2018 07 4;13(1):108. Epub 2018 Jul 4.

Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado Hospital, 12605 E. 16th St, Aurora, CO, 80045, USA.

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http://dx.doi.org/10.1186/s13023-018-0858-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031112PMC
July 2018

Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency.

Genet Med 2017 09 13;19(9):967-974. Epub 2017 Apr 13.

Department of Pediatrics Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, USA.

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http://dx.doi.org/10.1038/gim.2017.7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589980PMC
September 2017

Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.

Pediatr Transplant 2016 Sep 21;20(6):756-69. Epub 2016 Jun 21.

Departments of Pediatrics, Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

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http://dx.doi.org/10.1111/petr.12741DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5142218PMC
September 2016

Clearance of Hepatic Sphingomyelin by Olipudase Alfa Is Associated With Improvement in Lipid Profiles in Acid Sphingomyelinase Deficiency.

Am J Surg Pathol 2016 09;40(9):1232-42

Departments of *Pathology †Clinical Development, Sanofi Genzyme, Cambridge ¶Division of Genetics, Children's Hospital Boston #Department of Pediatrics, Harvard Medical School, Boston, MA ‡Division of Pediatric Genetic Medicine, The Children's Hospital at Montefiore, Bronx ∥Division of Liver Diseases, Mount Sinai School of Medicine, NY, NY §Manchester Centre for Genomic Medicine, St Mary's Hospital, CMFT, University of Manchester, Manchester, UK.

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http://dx.doi.org/10.1097/PAS.0000000000000659DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987207PMC
September 2016

Long-term follow-up in newborn screening: the role of collaboration.

Genet Med 2016 Aug 25. Epub 2016 Aug 25.

Department of Pediatrics, The Children's Hospital at Montefiore and the Albert Einstein College of Medicine, Bronx, New York, USA.

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http://dx.doi.org/10.1038/gim.2016.99DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383523PMC
August 2016

Screening of Newborns for Disorders with High Benefit-Risk Ratios Should Be Mandatory.

J Law Med Ethics 2016 06;44(2):231-40

Nicole Kelly, M.P.H., is the Research Program Manager for the Pilot Newborn Screening for Lysosomal Storage Disorders at the Albert Einstein College of Medicine. She is the Research Manager for the Division of Pediatric Genetic Medicine at the Children's Hospital at Montefiore. Dalia Chehayeb Makarem, M.P.H., is the Clinical Research Coordinator for the Pilot Newborn Screening for Lysosomal Storage Disorders at the Icahn School of Medicine at Mount Sinai. Melissa P. Wasserstein, M.D., is an Associate Professor of Pediatrics at the Albert Einstein College of Medicine and the Chief of Pediatric Genetic Medicine at The Children's Hospital at Montefiore in the Bronx, NY. She is a clinical biochemical geneticist, specializing in the care of individuals with rare inborn errors of metabolism.

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http://dx.doi.org/10.1177/1073110516654133DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381153PMC
June 2016

Types A and B Niemann-Pick Disease.

Pediatr Endocrinol Rev 2016 Jun;13 Suppl 1:674-81

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June 2016

Types A and B Niemann-Pick disease.

Best Pract Res Clin Endocrinol Metab 2015 Mar 16;29(2):237-47. Epub 2014 Oct 16.

Department of Genetics & Genomic Sciences, Ichan School of Medicine at Mount Sinai, 1428 Madison Avenue, 1st Floor, Room AB1-12, New York, NY 10029, United States. Electronic address:

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http://dx.doi.org/10.1016/j.beem.2014.10.002DOI Listing
March 2015

Neurologic and neurodevelopmental phenotypes in young children with early-treated combined methylmalonic acidemia and homocystinuria, cobalamin C type.

Mol Genet Metab 2013 Nov 25;110(3):241-7. Epub 2013 Jul 25.

Departments of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2013.07.018DOI Listing
November 2013

Morbidity and mortality in type B Niemann-Pick disease.

Genet Med 2013 Aug 14;15(8):618-23. Epub 2013 Feb 14.

Department of Pediatrics, Stony Brook School of Medicine, Stony Brook, New York, USA.

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http://dx.doi.org/10.1038/gim.2013.4DOI Listing
August 2013

Identification and characterization of eight novel SMPD1 mutations causing types A and B Niemann-Pick disease.

Mol Med 2010 Jul-Aug;16(7-8):316-21. Epub 2010 Apr 6.

Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine of New York University, New York, New York 10029, United States of America.

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http://dx.doi.org/10.2119/molmed.2010.00017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896470PMC
November 2010

Imaging manifestations of Niemann-Pick disease type B.

AJR Am J Roentgenol 2010 Jan;194(1):W12-9

Department of Radiology, Mount Sinai Medical Center, Box 1234, 1 Gustave L. Levy Pl., New York, NY 10029, USA.

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http://dx.doi.org/10.2214/AJR.09.2871DOI Listing
January 2010

High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria.

Mol Genet Metab 2009 Dec 12;98(4):344-8. Epub 2009 Aug 12.

Mount Sinai School of Medicine, Department of Pediatrics, Division of Pediatric Cardiology, NY 10029, USA.

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http://dx.doi.org/10.1016/j.ymgme.2009.07.017DOI Listing
December 2009

Resolution of cor pulmonale after medical management in a patient with cblC-type methylmalonic aciduria and homocystinuria: a case report.

Cases J 2009 Jul 30;2:8603. Epub 2009 Jul 30.

1Department of Pediatrics, Division of Pediatric Cardiology, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, Box 1201, New York, New York 10029, USA.

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http://dx.doi.org/10.4076/1757-1626-2-8603DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740237PMC
July 2009

Combined liver-kidney transplant for the management of methylmalonic aciduria: a case report and review of the literature.

Mol Genet Metab 2008 Jan 26;93(1):22-9. Epub 2007 Oct 26.

Department of Pediatrics, Mt. Sinai Medical Center, One Gustave L. Levy Place, New York, NY 10021, USA.

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http://dx.doi.org/10.1016/j.ymgme.2007.08.119DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786260PMC
January 2008

Acid sphingomyelinase deficiency: prevalence and characterization of an intermediate phenotype of Niemann-Pick disease.

J Pediatr 2006 Oct;149(4):554-9

Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA.

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http://dx.doi.org/10.1016/j.jpeds.2006.06.034DOI Listing
October 2006

Ocular manifestations of Niemann-Pick disease type B.

Ophthalmology 2004 Jul;111(7):1424-7

Department of Human Genetics and Pediatrics, Mount Sinai School of Medicine, New York, New York 10029, USA.

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http://dx.doi.org/10.1016/j.ophtha.2003.10.034DOI Listing
July 2004

Biochemical effect of intravenous arginine butyrate in X-linked adrenoleukodystrophy.

J Pediatr 2003 Jun;142(6):709-13

Department of Human Genetics, Mount Sinai School of Medicine, New York City, New York, USA.

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http://dx.doi.org/10.1067/mpd.2003.201DOI Listing
June 2003

Growth restriction in children with type B Niemann-Pick disease.

J Pediatr 2003 Apr;142(4):424-8

Department of Human Genetics, and the Carl C. Icahn Institute for Gene Therapy and Molecular Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.

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http://dx.doi.org/10.1067/mpd.2003.113DOI Listing
April 2003