ParthaSGhoshMD

PubMed

• 1 citations
  Single-institution Series of Hirayama Disease in North America.
  Benjamin T Lynch, Anna L Slingerland, Partha S Ghosh, Daniel J Hedequist, Mark R Proctor, Katie P Fehnel, Robson, C. D., Caroline D Robson> ;Clinical Spine Surgery. 2024 Feb 1
• Variants in DTNA cause a mild, dominantly inherited muscular dystrophy.
  Andres Nascimento, Christine C Bruels, Sandra Donkervoort, A Reghan Foley, Anna Codina, Jose C Milisenda, Elicia A Estrella, Chengcheng Li, Jordi Pijuan, Isabelle Drap...> ;Acta Neuropathologica. 2023 Apr 1
• Upper motor neuron signs and early onset gait abnormalities in young children with bi-allelic VWA1 variants.
  Dustin L Gable, Alisa Mo, Elicia Estrella, Afshin Saffari, Partha S Ghosh, Darius Ebrahimi-Fakhari> ;American Journal of Medical Genetics. Part A. 2022 Dec 1
• 11 citations
  Diagnostic capabilities of nanopore long-read sequencing in muscular dystrophy.
  Christine C Bruels, Hannah R Littel, Audrey L Daugherty, Seth Stafki, Elicia A Estrella, Emily S McGaughy, Don Truong, Jonathan P Badalamenti, Lynn Pais, Vijay S Ganes...> ;Annals of Clinical and Translational Neurology. 2022 Aug 1
• A Boy with Herculean Appearance.
  Sarah Wright, Partha S Ghosh> ;The Journal of Pediatrics. 2022 May 1
• Unilateral Cavovarus Foot From Sciatic Nerve Perineurioma.
  Regina Laine, Tal Laor, Partha S Ghosh> ;Neurology India. 2022 Mar 10
• "Spokes of Wheel" in Muscle Biopsy.
  Luisa F Angel Buitrago, Hart G W Lidov, Partha S Ghosh> ;Journal of Clinical Neuromuscular Disease. 2022 Mar 1
• 7 citations
  BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy.
  Sandra Donkervoort, Niklas Krause, Mykola Dergai, Pomi Yun, Judith Koliwer, Svetlana Gorokhova, Janelle Geist Hauserman, Beryl B. Cummings, Ying Hu, Rosemarie Smith, P...> ;EMBO Molecular Medicine. 2021 Nov 15
• 6-month old with new-onset weakness: consider infant botulism.
  Luisa Angel Buitrago, Partha S. Ghosh> ;Archives of Disease in Childhood. 2021 Sep 3
• Myasthenia Gravis in a Child After Graft-versus-Host Disease.
  Devin E Prior, Partha S. Ghosh> ;Journal of Clinical Neuromuscular Disease. 2021 Sep 1
• Postsurgical Inflammatory Sciatic Neuropathy
  Devin E Prior, Partha S. Ghosh> ;Journal of Clinical Neuromuscular Disease. 2021 Jun 1
• Aphasia and Weakness in a Child Think Beyond Stroke.
  Devin E Prior, Partha S. Ghosh> ;Journal of Clinical Neuromuscular Disease. 2021 Jun 1
• 2 citations
  Electromyography in infants: experience from a pediatric neuromuscular center
  Obehioya Irumudomon, Partha S. Ghosh> ;Acta Neurologica Belgica. 2021 Apr 23
• Developing outcome measures of disease activity in Pediatric Myasthenia.
  Devin E Prior, Bo Zhang, Partha S. Ghosh> ;Muscle & Nerve. 2021 Feb 18
• 9 citations
  Congenital Myasthenic Syndrome From a Single Center: Phenotypic and Genotypic features.
  Devin E Prior, Partha S. Ghosh> ;Journal of Child Neurology. 2021 Jan 20
• 3 citations
  Neuroimage: the crescent moon sign of Hirayama disease.
  Devin E Prior, Partha S. Ghosh> ;Acta Neurologica Belgica. 2021 Jan 2
• 1 citations
  Clinical Reasoning: A 10-year-old girl with muscle stiffness.
  Devin E Prior, Partha S. Ghosh> ;Neurology. 2020 Aug 11
• 20 citations
  Update on Muscular Dystrophies with Focus on Novel Treatments and Biomarkers
  Neil Datta, Partha S. Ghosh> ;Current Neurology and Neuroscience Reports. 2020 May 14
• 1 citations
  Clinical Reasoning: Seven-year-old girl with progressive gait difficulties.
  Jillian Alderson, Partha S. Ghosh> ;Neurology. 2020 Feb 25
• Response to “The Spectrum of Neuromuscular Disorders Admitted to a Pediatric Intensive Care Unit Is Broader Than Anticipated”:
  Dana B. Harrar, Basil T. Darras, Partha S. Ghosh> ;Journal of Child Neurology. 2020 Jan 3
• 8 citations
  Acute Neuromuscular Disorders in the Pediatric Intensive Care Unit.
  Dana B. Harrar, Basil T. Darras, Partha S. Ghosh> ;Journal of Child Neurology. 2019 Sep 10
• 1 citations
  Clinical Reasoning: Pes cavus and neuropathy: Think beyond Charcot-Marie-Tooth disease
  Jillian Alderson, Partha S. Ghosh> ;Neurology. 2019 Aug 20
• 7 citations
  Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites.
  Christine C. Bruels, Chengcheng Li, Tonatiuh Mendoza, Jamillah Khan, Hemakumar M. Reddy, Elicia Estrella, Partha S. Ghosh, Basil T. Darras, Hart G.W. Lidov, Christina ...> ;Molecular Genetics & Genomic Medicine. 2019 Mar 1
• 72 citations
  Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration
  Vandana Shashi, Maria M. Magiera, Dennis Klein, Maha S. Zaki, Kelly Schoch, Sabine Rudnik-Schöneborn, A. Norman, Osorio Abath Neto, Marina Dusl, Xidi Yuan, Luca Bartes...> ;The EMBO Journal. 2018 Dec 3
• Clinical Reasoning: Young adult with dysphagia and severe weight loss.
  Obehioya Irumudomon, Partha S. Ghosh> ;Neurology. 2018 Sep 11
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Journal Articles

• Diagnostic yield of electromyography in children with myopathic disorders.  
  Ghosh PS, Sorenson EJ, Pediatric Neurology, 8/1/2014