Neuroimaging manifestations and classification of congenital muscular dystrophies.

Congenital progressive muscular dystrophy of the fukuyama type — clinical, genetic and pathological considerations —

1981 • 469 citations

Congenital muscular dystrophy with merosin deficiency.

1994 • 449 citations

Formation, maturation, and disorders of brain neocortex.

1992 • 249 citations

Relationship between neuronal migration and cell-substratum adhesion: laminin and merosin promote olfactory neuronal migration but are anti-adhesive.

1991 • 204 citations

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

1994 • 195 citations

Muscle—eye—brain disease: A neuropathological study

1997 • 166 citations

Syndromes with lissencephaly. II: Walker‐Warburg and Cerebro‐Oculo‐Muscular syndromes and a new syndrome with type II lissencephaly

1985 • 154 citations

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities

1997 • 152 citations

Muscle, Eye and Brain Disease: A New Syndrome

1977 • 128 citations

Cerebro‐ocular dysgenesis (Walker‐Warburg syndrome)

1984 • 122 citations

Merosin promotes cell attachment and neurite outgrowth and ls a component of the neurite-promoting factor of RN22 schwannoma cells

1992 • 90 citations

Brain MR in Fukuyama congenital muscular dystrophy.

1996 • 78 citations

Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker‐Warburg syndrome (cerebroocular dysplasia‐muscular dystrophy)

1995 • 66 citations

MRI of the brain in muscle-eye-brain (MEB) disease

1994 • 63 citations

Muscle-eye-brain disease

1998 • 60 citations

N-cadherin expression and function in cultured oligodendrocytes

1996 • 56 citations

Involvement of the Central Nervous System in Congenital Muscular Dystrophies

1983 • 55 citations

Genetic identity of Fukuyama‐type congenital muscular dystrophy and Walker‐Warburg syndrome

1995 • 53 citations

Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

1997 • 50 citations

Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.

1998 • 47 citations

Cerebellar MR in Fukuyama congenital muscular dystrophy: polymicrogyria with cystic lesions.

1994 • 44 citations

Preserved Merosin M-Chain (or Laminin-α₂) Expression in Skeletal Muscle Distinguishes Walker-Warburg Syndrome from Fukuyama Muscular Dystrophy and Merosin-Deficient Congenital Muscular Dystrophy

1995 • 44 citations

Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency.

1996 • 38 citations

Cerebellar micropolygyria in fukuyama congenital muscular dystrophy: Observations in fetal and pediatric cases

1990 • 36 citations

Congenital muscular dystrophy: brain alterations in an unselected series of Western patients.

1991 • 35 citations

Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis

1988 • 34 citations

Occidental type cerebromuscular dystrophy: a report of eleven cases.

1991 • 34 citations

Neuropathological findings in muscle-eye-brain disease (MEB-D)

1991 • 30 citations

Classification of the cerebro-oculo-muscular syndrome(s)

1993 • 23 citations

Congenital Muscular Dystrophy with Cerebral Involvement - Report of a Case of "Occidental Type Cerebromuscular Dystrophy"?

1990 • 17 citations

Analysis of "Pure" Congenital Muscular Dystrophies in Thirty-Eight Cases. How Different is the Classical Type 1 from the Occidental Type Cerebromuscular Dystrophy?

1994 • 17 citations