Literature DB >> 25684057

Disease specific therapies in leukodystrophies and leukoencephalopathies.

Guy Helman1, Keith Van Haren2, Joshua L Bonkowsky3, Genevieve Bernard4, Amy Pizzino2, Nancy Braverman5, Dean Suhr6, Marc C Patterson7, S Ali Fatemi8, Jeff Leonard9, Marjo S van der Knaap10, Stephen A Back11, Stephen Damiani12, Steven A Goldman13, Asako Takanohashi14, Magdalena Petryniak15, David Rowitch16, Albee Messing17, Lawrence Wrabetz18, Raphael Schiffmann19, Florian Eichler20, Maria L Escolar21, Adeline Vanderver22.   

Abstract

Leukodystrophies are a heterogeneous, often progressive group of disorders manifesting a wide range of symptoms and complications. Most of these disorders have historically had no etiologic or disease specific therapeutic approaches. Recently, a greater understanding of the pathologic mechanisms associated with leukodystrophies has allowed clinicians and researchers to prioritize treatment strategies and advance research in therapies for specific disorders, some of which are on the verge of pilot or Phase I/II clinical trials. This shifts the care of leukodystrophy patients from the management of the complex array of symptoms and sequelae alone to targeted therapeutics. The unmet needs of leukodystrophy patients still remain an overwhelming burden. While the overwhelming consensus is that these disorders collectively are symptomatically treatable, leukodystrophy patients are in need of advanced therapies and if possible, a cure.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Care; Consensus; Leukodystrophy; Outcomes; Prevention; Therapy

Mesh:

Year:  2015        PMID: 25684057      PMCID: PMC4390468          DOI: 10.1016/j.ymgme.2015.01.014

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  79 in total

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3.  Early use of drastic therapy.

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Journal:  Hum Mol Genet       Date:  2012-03-02       Impact factor: 6.150

5.  Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo's oil.

Authors:  Hugo W Moser; Gerald V Raymond; Shou-En Lu; Larry R Muenz; Ann B Moser; Jiahong Xu; Richard O Jones; Daniel J Loes; Elias R Melhem; Prachi Dubey; Lena Bezman; N Hong Brereton; Augusto Odone
Journal:  Arch Neurol       Date:  2005-07

6.  Neural stem cell engraftment and myelination in the human brain.

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Journal:  Sci Transl Med       Date:  2012-10-10       Impact factor: 17.956

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Journal:  Sci Transl Med       Date:  2012-10-10       Impact factor: 17.956

8.  PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease.

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9.  Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.

Authors:  C Walter; J Gootjes; P A Mooijer; H Portsteffen; C Klein; H R Waterham; P G Barth; J T Epplen; W H Kunau; R J Wanders; G Dodt
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10.  An autoimmune disease prevented by anti-retroviral drugs.

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  15 in total

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3.  Modeling the Mutational and Phenotypic Landscapes of Pelizaeus-Merzbacher Disease with Human iPSC-Derived Oligodendrocytes.

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Journal:  Exp Neurol       Date:  2016-05-08       Impact factor: 5.330

6.  Novel and known morbidities of leukodystrophies identified using a phenome-wide association study.

Authors:  Joshua L Bonkowsky; Jacob Wilkes; Jian Ying; Wei-Qi Wei
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7.  Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophies.

Authors:  Laura A Adang; Omar Sherbini; Laura Ball; Miriam Bloom; Anil Darbari; Hernan Amartino; Donna DiVito; Florian Eichler; Maria Escolar; Sarah H Evans; Ali Fatemi; Jamie Fraser; Leslie Hollowell; Nicole Jaffe; Christopher Joseph; Mary Karpinski; Stephanie Keller; Ryan Maddock; Edna Mancilla; Bruce McClary; Jana Mertz; Kiley Morgart; Thomas Langan; Richard Leventer; Sumit Parikh; Amy Pizzino; Erin Prange; Deborah L Renaud; William Rizzo; Jay Shapiro; Dean Suhr; Teryn Suhr; Davide Tonduti; Jacque Waggoner; Amy Waldman; Nicole I Wolf; Ayelet Zerem; Joshua L Bonkowsky; Genevieve Bernard; Keith van Haren; Adeline Vanderver
Journal:  Mol Genet Metab       Date:  2017-08-20       Impact factor: 4.797

Review 8.  Adulthood leukodystrophies.

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9.  Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter Disorders.

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