Related references
Note: Only part of the references are listed.Long-term outcomes after allogeneic hematopoietic stem cell transplantation for metachromatic leukodystrophy: the largest single-institution cohort report
Alexander A. Boucher et al.
ORPHANET JOURNAL OF RARE DISEASES (2015)
Critical issues for the proper diagnosis of Metachromatic Leukodystrophy
Laura Lorioli et al.
GENE (2014)
Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort
Christiane Kehrer et al.
ORPHANET JOURNAL OF RARE DISEASES (2014)
Neurodevelopmental Outcomes of Umbilical Cord Blood Transplantation in Metachromatic Leukodystrophy
Holly R. Martin et al.
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION (2013)
Sixteen novel mutations in the arylsulfatase A gene causing metachromatic leukodystrophy
Paola Luzi et al.
GENE (2013)
Gallbladder polyposis in metachromatic leukodystrophy
Aanchal Agarwal et al.
PEDIATRIC RADIOLOGY (2013)
Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy
Alessandra Biffi et al.
SCIENCE (2013)
Improvement of White Matter Changes on Neuroimaging Modalities After Stem Cell Transplant in Metachromatic Leukodystrophy
Martje E. van Egmond et al.
JAMA NEUROLOGY (2013)
Multi-Voxel 1H-MRs in Metachromatic Leukodystrophy
Mitra Assadi et al.
JOURNAL OF CENTRAL NERVOUS SYSTEM DISEASE (2013)
Toward a Better Understanding of Brain Lesions during Metachromatic Leukodystrophy Evolution
A. Martin et al.
AMERICAN JOURNAL OF NEURORADIOLOGY (2012)
Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy
Yo Niida et al.
JOURNAL OF HUMAN GENETICS (2012)
Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy
Samuel Groeschel et al.
NEUROLOGY (2012)
The natural course of gross motor deterioration in metachromatic leukodystrophy
Christiane Kehrer et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2011)
Childhood leukodystrophies: a clinical perspective
Alfried Kohlschuetter et al.
EXPERT REVIEW OF NEUROTHERAPEUTICS (2011)
Lysosomal storage diseases: Diagnostic confirmation and management of presymptomatic individuals
Raymond Y. Wang et al.
GENETICS IN MEDICINE (2011)
Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course
Samuel Groeschel et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2011)
Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population
Pallavi Shukla et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2011)
Metachromatic Leukodystrophy: A Case of Triplets With the Late Infantile Variant and a Systematic Review of the Literature
Asif Mahmood et al.
JOURNAL OF CHILD NEUROLOGY (2010)
Identification of a Novel Splicing Mutation in the ARSA Gene in a Patient with Late-infantile Form of Metachromatic Leukodystrophy
Dong-Hee Kang et al.
KOREAN JOURNAL OF LABORATORY MEDICINE (2010)
ARSA gene mutations in five Chinese metachromatic leukodystrophy patients
Jingmin Wang et al.
PEDIATRIC NEUROLOGY (2007)
Peripheral neuropathy in metachromatic leucodystrophy. A study of 40 cases from south India
PS Bindu et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2005)
Spinal cord and cauda equina MRI findings in metachromatic leukodystrophy: case report
I Toldo et al.
NEURORADIOLOGY (2005)
Multifocal slowing of nerve conduction in metachromatic leukodystrophy
CL Cameron et al.
MUSCLE & NERVE (2004)
Metachromatic leukodystrophy: Recent research developments
V Gieselmann
JOURNAL OF CHILD NEUROLOGY (2003)
Disease-causing mutations in cis with the common arylsulfatase A pseudodeficiency allele compound the difficulties in accurately identifying patients and carriers of metachromatic leukodystrophy
MA Rafi et al.
MOLECULAR GENETICS AND METABOLISM (2003)
Increased prevalence of pervasive developmental disorders in children with slight arylsulfatase A deficiency
MG Alessandri et al.
BRAIN & DEVELOPMENT (2002)
Share Paper
