Publications by authors named "Sumit Parikh"

60Publications

Mitochondrial diseases in North America: An analysis of the NAMDC Registry.

Neurol Genet 2020 Apr 2;6(2):e402. Epub 2020 Mar 2.

Department of Neurology (E.B., V.E., S.D., K.E., X.Q.R., M.H.), Columbia University Medical Center, New York; Department of Biostatistics (Y.L., V.C., J.K., J. Grier, R.B., J.L.P.T.), Mailman School of Public Health, Columbia University, New York; Radboudumc (R.S.), Nijmegen, The Netherlands; Department of Pediatrics (B.H.C.), Northeast Ohio Medical University and Akron Children's Hospital; Genetics Unit (A.K.), Massachusetts General Hospital, Boston; Department of Pediatrics (G.D.V.), State University of New York at Buffalo; Departments of Neurosciences and Pediatrics (R.H.), University of California at San Diego; Department of Pediatrics (J.L.K.V.H., A.L.), University of Colorado School of Medicine, Aurora; Department of Molecular and Human Genetics (F.S.), Baylor College of Medicine, Houston, TX; Texas Children's Hospital (F.S.), Houston; Joint BCM-CUHK Center of Medical Genetics (F.S.), Prince of Wales Hospital, ShaTin, New Territories, Hong Kong; Department of Neurology (S.P.), Cleveland Clinic, OH; Departments of Genetics and Genome Sciences and Pediatrics (J.K.B., S.D.D.), and Center for Human Genetics, University Hospitals Cleveland Medical Center, Case Western Reserve University, OH; Departments of Neurology and Clinical Genomics (R.H.G.), Mayo Clinic, Rochester, MN; Department of Neurology (R.P.S.), University of Washington, Seattle Children's Hospital; Department of Pediatrics (G.M.E.), Stanford University, Palo Alto, CA; Department of Medicine (P.W.S.), University of Florida at Gainesville; Genetics and Genomic Sciences at the Icahn School of Medicine at Mount Sinai (J. Ganesh), New York; Mitochondrial Medicine Frontier Program (Z.Z.-C., M.J.F., A.C.G.), Division of Human Genetics, The Children's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine; University of Pennsylvania Perelman School of Medicine (Z.Z.-C.), Philadelphia; Department of Neurology (M.T.), McMasters University, Toronto, Ontario, Canada; Department of Neurology (A.G.), Children's National Health Network, Washington, DC; Office of Dietary Supplements (K.C.), National Institutes of Health, Bethesda, MD; and Eunice Kennedy Shriver National Institute of Child Health and Human Development (D.K.), National Institutes of Health, Bethesda, MD.

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http://dx.doi.org/10.1212/NXG.0000000000000402DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164977PMC
April 2020

The Australian experience with switching to extended half-life factor VIII and IX concentrates: On behalf of the Australian Haemophilia Centre Directors' Organisation.

Haemophilia 2020 May 3;26(3):529-535. Epub 2020 Apr 3.

Australian Haemophilia Centre Directors Organisation (AHCDO), Melbourne, Vic., Australia.

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http://dx.doi.org/10.1111/hae.13970DOI Listing
May 2020

Fatigue in primary genetic mitochondrial disease: No rest for the weary.

Neuromuscul Disord 2019 11 25;29(11):895-902. Epub 2019 Sep 25.

Mitochondrial Disease Program, Genetics Unit, Massachusetts General Hospital, Boston, MA, United States.

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http://dx.doi.org/10.1016/j.nmd.2019.09.012DOI Listing
November 2019

Primary mitochondrial disease in the US: Data from patients and physicians' perspective on health care delivery.

Data Brief 2019 Aug 30;25:104343. Epub 2019 Jul 30.

Neurogenetics, Center for Pediatric Neurology, Cleveland Clinic Children's Hospital, Cleveland, OH, USA.

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http://dx.doi.org/10.1016/j.dib.2019.104343DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727191PMC
August 2019

Severity Assessment in CDKL5 Deficiency Disorder.

Pediatr Neurol 2019 08 27;97:38-42. Epub 2019 Mar 27.

Children's Hospital Colorado and University of Colorado School of Medicine Aurora, Colorado; Department of Pediatrics, Aurora, Colorado; Department of Pharmacology, Aurora, Colorado; Department of Neurology, Aurora, Colorado; Department of Otolaryngology, Aurora, Colorado. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2019.03.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659999PMC
August 2019

Harmonizing care for rare diseases: How we developed the mitochondrial care network in the United States.

Mol Genet Metab 2019 06 23;127(2):122-127. Epub 2019 May 23.

Neurogenetics, Center for Pediatric Neurology, Cleveland Clinic Children's Hospital, Cleveland, OH, United States of America.

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http://dx.doi.org/10.1016/j.ymgme.2019.05.012DOI Listing
June 2019

Complication rates of central venous access devices in patients with inherited bleeding disorders in Australia.

Br J Haematol 2019 08 2;186(4):e86-e88. Epub 2019 Apr 2.

Australian Centre for Blood Diseases, Monash University Alfred Hospital, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1111/bjh.15914DOI Listing
August 2019

A physician targeted intervention improves prescribing in chronic heart failure in general medical units.

BMC Health Serv Res 2018 03 23;18(1):206. Epub 2018 Mar 23.

Department of Medicine, Northern Health, 185 Cooper Street, Epping, VIC, Australia.

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http://dx.doi.org/10.1186/s12913-018-3009-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865296PMC
March 2018

Inborn Errors of Metabolism with Movement Disorders: Defects in Metal Transport and Neurotransmitter Metabolism.

Pediatr Clin North Am 2018 04;65(2):301-315

Department of Neurology, Neurological Institute, Center for Pediatric Neurology, Cleveland Clinic, 9500 Euclid Avenue, S60, Cleveland, OH 44195, USA. Electronic address:

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http://dx.doi.org/10.1016/j.pcl.2017.11.010DOI Listing
April 2018

Orbital rhabdomyosarcoma in a child with Leigh syndrome.

J AAPOS 2018 04 20;22(2):150-152.e1. Epub 2017 Dec 20.

Department of Ophthalmology, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.

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https://linkinghub.elsevier.com/retrieve/pii/S10918531173031
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http://dx.doi.org/10.1016/j.jaapos.2017.09.006DOI Listing
April 2018

Disparities in access to anti-vascular endothelial growth factor treatment for neovascular age-related macular degeneration.

Clin Exp Ophthalmol 2017 Mar 12;45(2):143-151. Epub 2016 Sep 12.

Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ceo.12804DOI Listing
March 2017

Mitochondrial disease patients' perception of dietary supplements' use.

Mol Genet Metab 2016 09 16;119(1-2):100-8. Epub 2016 Jul 16.

Department of Neurology, Columbia University Medical Center, New York, NY 10032, United States. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2016.07.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031526PMC
September 2016

Authors' response to Finsterer and Zarrouk-Mahjoub's comments.

Ophthalmic Genet 2017 May-Jun;38(3):299. Epub 2016 Jul 21.

c Cleveland Clinic, Cole Eye Institute, Center for Genetic Eye Diseases , Cleveland , Ohio , USA.

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http://dx.doi.org/10.1080/13816810.2016.1193882DOI Listing
January 2018

Ophthalmological findings in 74 patients with mitochondrial disease.

Ophthalmic Genet 2017 Jan-Feb;38(1):67-69. Epub 2016 Mar 30.

a Cleveland Clinic , Center for Pediatric Neurology , Cleveland , Ohio , USA.

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http://dx.doi.org/10.3109/13816810.2015.1130153DOI Listing
November 2017

Recommendations for the Management of Strokelike Episodes in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes.

JAMA Neurol 2016 May;73(5):591-4

Department of Pediatrics, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

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http://dx.doi.org/10.1001/jamaneurol.2015.5072DOI Listing
May 2016

Electrographic status epilepticus in sleep in an adult with cerebral folate deficiency.

Neurol Clin Pract 2016 Feb;6(1):e4-e7

Epilepsy Center (UT, PK, ANVM, AG, EMPK) and Pediatric Neurology Section (PS), Cleveland Clinic, Cleveland, OH.

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http://dx.doi.org/10.1212/CPJ.0000000000000199DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753830PMC
February 2016

Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathy.

Ann Clin Transl Neurol 2016 Feb 21;3(2):114-23. Epub 2015 Dec 21.

Department of Human Genetics University of Michigan Ann Arbor Michigan.

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http://dx.doi.org/10.1002/acn3.276DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748308PMC
February 2016

Migraine Variants or Episodic Syndromes That May Be Associated With Migraine and Other Unusual Pediatric Headache Syndromes.

Headache 2016 Jan;56(1):206-14

Cleveland Clinic Foundation, Cleveland, OH, USA.

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http://dx.doi.org/10.1111/head.12750DOI Listing
January 2016

Relationship between health-related quality of life, comorbidities and acute health care utilisation, in adults with chronic conditions.

Health Qual Life Outcomes 2015 May 29;13:69. Epub 2015 May 29.

Northern Clinical Research Centre, Northern Health, 185 Cooper Street, 3076, Epping, Victoria, Australia.

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http://dx.doi.org/10.1186/s12955-015-0260-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446844PMC
May 2015

Exploring in-hospital adverse drug events using ICD-10 codes.

Aust Health Rev 2014 Sep;38(4):454-60

Northern Clinical Research Centre, Northern Health, 185 Cooper Street, Epping, Vic. 3076, Australia. Email:

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http://dx.doi.org/10.1071/AH13166DOI Listing
September 2014

Approach to the diagnosis and treatment of cyclic vomiting syndrome: a large single-center experience with 106 patients.

Pediatr Neurol 2014 Jun 21;50(6):569-73. Epub 2014 Feb 21.

Center for Pediatric Neurology and Neurosurgery, The Cleveland Clinic, Cleveland, Ohio; Program for Pediatric Neurometabolism/Neurogenetics, The Cleveland Clinic, Cleveland, Ohio. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08878994140013
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http://dx.doi.org/10.1016/j.pediatrneurol.2014.02.009DOI Listing
June 2014

Treatment of mitochondrial disorders.

Curr Treat Options Neurol 2014 Jun;16(6):292

Department of Neurology, Cleveland Clinic, Cleveland, OH, USA,

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http://dx.doi.org/10.1007/s11940-014-0292-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067597PMC
June 2014

Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and management.

Mitochondrion 2013 Nov 21;13(6):681-7. Epub 2013 Sep 21.

Center for Child Neurology, Cleveland Clinic Children's Hospital, Cleveland, OH, United States. Electronic address:

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http://dx.doi.org/10.1016/j.mito.2013.09.003DOI Listing
November 2013

Autonomic dysfunction in epilepsy and mitochondrial diseases.

Semin Pediatr Neurol 2013 Mar;20(1):31-4

Neurological Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1016/j.spen.2013.01.003DOI Listing
March 2013

Neurologic disorders due to mitochondrial DNA mutations.

Semin Pediatr Neurol 2012 Dec;19(4):194-202

Center for Human Genetics, University Hospitals, Case Medical Center, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1016/j.spen.2012.09.006DOI Listing
December 2012

Late infantile neuronal ceroid lipofuscinosis and dopamine deficiency.

J Child Neurol 2012 Feb 22;27(2):234-7. Epub 2011 Sep 22.

Center for Pediatric Neurology, Cleveland Clinic, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1177/0883073811419261DOI Listing
February 2012

The neurologic manifestations of mitochondrial disease.

Authors:
Sumit Parikh

Dev Disabil Res Rev 2010 ;16(2):120-8

Neurogenetics and Metabolism, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1002/ddrr.110DOI Listing
January 2011

A modern approach to the treatment of mitochondrial disease.

Curr Treat Options Neurol 2009 Nov;11(6):414-30

Sumit Parikh, MD Neurometabolism & Neurogenetics, Cleveland Clinic, 9500 Euclid Avenue, S71, Cleveland, OH 44195, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561461PMC
http://dx.doi.org/10.1007/s11940-009-0046-0DOI Listing
November 2009

Vitamins, not surgery: spinal fluid testing in hemispheric epilepsy.

Pediatr Neurol 2009 Jun;40(6):477-9

Centers for Pediatric Neurology & Epilepsy, Neuroscience Institute, Cleveland Clinic, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1016/j.pediatrneurol.2009.01.007DOI Listing
June 2009

Otolaryngologic manifestations of mitochondrial cytopathies.

Am J Otolaryngol 2009 May-Jun;30(3):162-5. Epub 2008 Oct 1.

Department of Otolaryngology, Washington University, School of Medicine, St Louis, MO 63130, USA.

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http://dx.doi.org/10.1016/j.amjoto.2008.04.008DOI Listing
July 2009

Aicardi syndrome in a genotypic male.

Ophthalmic Genet 2008 Dec;29(4):181-3

Cleveland Clinic, Cole Eye Institute, Cleveland 44195, USA.

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http://dx.doi.org/10.1080/13816810802320209DOI Listing
December 2008

Metabolic testing in the pediatric epilepsy unit.

Pediatr Neurol 2008 Mar;38(3):191-5

Center for Pediatric Neurology, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1016/j.pediatrneurol.2007.10.011DOI Listing
March 2008

The in-depth evaluation of suspected mitochondrial disease.

Mol Genet Metab 2008 May 1;94(1):16-37. Epub 2008 Feb 1.

Department of Neurosciences, University of California San Diego, La Jolla, CA and Rady Children's Hospital San Diego, San Diego, CA, United States.

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http://dx.doi.org/10.1016/j.ymgme.2007.11.018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810849PMC
May 2008

Mitochondrial disease: a practical approach for primary care physicians.

Pediatrics 2007 Dec;120(6):1326-33

Department of Neurosciences, University of California San Diego, 9500 Gilman Dr, La Jolla, CA 92093-0935, USA.

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http://dx.doi.org/10.1542/peds.2007-0391DOI Listing
December 2007

Misplaced peripherally inserted central catheter: an unusual cause of stroke.

Pediatr Neurol 2004 Mar;30(3):210-2

Department of Child Neurology, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S088789940300475
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http://dx.doi.org/10.1016/j.pediatrneurol.2003.09.008DOI Listing
March 2004