Two brothers with Pelizaeus-Merzbacher disease presenting with neonatal hypotonia and hyporeflexia are reported from the Tuft’s University School of Medicine, and Massachusetts General Hospital, Boston, and the EKS Center for Mental Retardation, Waltham, MA
Pelizaeus-Merzbacher disease (PMD) is an X-linked recessive disorder affecting myelination of the ce...
International audiencePelizaeus-Merzbacher Disease is an X-linked hypomyelinatiing leukodystrophy. W...
We describe in two brothers an apparently novel syndrome comprising obesity, congenital hypothyroidi...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
Pelizaeus-Merzbacher disease (PMD) is a rare disorder with X-linked inheritance. The leading symptom...
Friedrich Pelizaeus provided the first clinical picture of the disease and managed to correctly iden...
Pelizaeus-Merzbacher disease is an X-linked recessive neurological disorder with nystagmus, ataxia, ...
Pelizaeus-Merzbacher Disease (PMD), a rare hereditary dysmyelinating disorder, may rarely masquerade...
Pelizaeus-Merzbacher disease is a rare disease of infants and young children in which there is an ar...
Pelizaeus-Merzbacher disease and X-linked spastic paraplegia type 2 are two sides of the same coin. ...
Thyroid hormones are essential for differentiation and function of oligodendrocytes, contributing to...
A family with X-linked inheritance and Pelizaeus-Merzbacher-like disease (PMLD), PMD without the pro...
Magnetic search-coil oculography of three brothers, aged 20, 22, and 25, with Pelizaeus-Merzbacher d...
Zellweger syndrome, a paradigm of human peroxisomal disorders is characterized by dysmorphic feature...
Pelizaeus-Merzbacher disease (PMD) is an X-linked recessive disorder affecting myelination of the ce...
International audiencePelizaeus-Merzbacher Disease is an X-linked hypomyelinatiing leukodystrophy. W...
We describe in two brothers an apparently novel syndrome comprising obesity, congenital hypothyroidi...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
Pelizaeus-Merzbacher disease (PMD) is a rare disorder with X-linked inheritance. The leading symptom...
Friedrich Pelizaeus provided the first clinical picture of the disease and managed to correctly iden...
Pelizaeus-Merzbacher disease is an X-linked recessive neurological disorder with nystagmus, ataxia, ...
Pelizaeus-Merzbacher Disease (PMD), a rare hereditary dysmyelinating disorder, may rarely masquerade...
Pelizaeus-Merzbacher disease is a rare disease of infants and young children in which there is an ar...
Pelizaeus-Merzbacher disease and X-linked spastic paraplegia type 2 are two sides of the same coin. ...
Thyroid hormones are essential for differentiation and function of oligodendrocytes, contributing to...
A family with X-linked inheritance and Pelizaeus-Merzbacher-like disease (PMLD), PMD without the pro...
Magnetic search-coil oculography of three brothers, aged 20, 22, and 25, with Pelizaeus-Merzbacher d...
Zellweger syndrome, a paradigm of human peroxisomal disorders is characterized by dysmorphic feature...
Pelizaeus-Merzbacher disease (PMD) is an X-linked recessive disorder affecting myelination of the ce...
International audiencePelizaeus-Merzbacher Disease is an X-linked hypomyelinatiing leukodystrophy. W...
We describe in two brothers an apparently novel syndrome comprising obesity, congenital hypothyroidi...
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