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Peripheral nerve and skeletal muscle involvement in CADASIL

Acta neuropathologica, 2005-12, Vol.110 (6), p.587-599

2005

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X-linked dominant Charcot-Marie-Tooth disease : nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)

Acta neuropathologica, 1998-05, Vol.95 (5), p.443-449

1998

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Morphological changes following experimental intraventricular haemorrhage and intraventricular fibrinolytic treatment with recombinant tissue plasminogen activator

Acta neuropathologica, 2000-11, Vol.100 (5), p.561-567

2000

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Comparative morphometric evaluation of peripheral nerves and muscle fibers in myotonic dystrophy

Acta neuropathologica, 2000-01, Vol.99 (1), p.39-47

2000

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Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency

Acta neuropathologica, 2004-08, Vol.108 (2), p.154-167

2004

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Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Acta neuropathologica, 1995-02, Vol.89 (2), p.116-121

1995

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Major histocompatibility complex class II expression by activated microglia caudal to lesions of descending tracts in the human spinal cord is not associated with a T cell response

Acta neuropathologica, 2000-11, Vol.100 (5), p.528-536

2000

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Demyelinating sensorimotor neuropathy with congenital cataract, mental retardation, and unique, dysplastic perineurial cells within the endoneurium

Acta neuropathologica, 1999-10, Vol.98 (4), p.421-426

1999

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Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)

Acta neuropathologica, 2004-09, Vol.108 (3), p.250-256

2004

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Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis)

Acta neuropathologica, 1993, Vol.85 (4), p.419-430

1993

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Screening for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsy in archival nerve biopsy samples by direct-double-differential PCR

Acta neuropathologica, 2000-11, Vol.100 (5), p.459-463

2000

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Polyneuropathy with osmiophilic membrane-bound, cytoplasmic inclusions in Schwann cells (POMCIS)

Acta neuropathologica, 1999-10, Vol.98 (4), p.427-432

1999

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Changes of the ratio between myelin thickness and axon diameter in human developing sural, femoral, ulnar, facial, and trochlear nerves

Acta neuropathologica, 1988-09, Vol.76 (5), p.471-483

1988

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Dominantly inherited myopathy with novel tubular aggregates containing 1-21 tubulofilamentous structures

Acta neuropathologica, 2001-07, Vol.102 (1), p.27-35

2001

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Inhibitory effects of thalidomide on cellular proliferation, endoneurial edema and myelin phagocytosis during early Wallerian degeneration

Acta neuropathologica, 1995-05, Vol.89 (5), p.415-419

1995

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Nuclear and mitochondrial changes of muscle fibers in AIDS after treatment with high doses of zidovudine

Acta neuropathologica, 1992-12, Vol.85 (1), p.39-47

1992

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Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions

Acta neuropathologica, 1998-07, Vol.96 (1), p.41-51

1998

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Fine structural evaluation of altered Schmidt-Lanterman incisures in human sural nerve biopsies

Acta neuropathologica, 1992, Vol.83 (2), p.120-133

1992

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Significance of degenerating endoneurial cells in peripheral neuropathy

Acta neuropathologica, 1991-01, Vol.81 (6), p.680-685

1991

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Correlation between the number of epineurial and endoneurial blood vessels in diseased human sural nerves

Acta neuropathologica, 2001-10, Vol.102 (4), p.364-372

2001

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Colchicine myopathy in a case of familial mediterranean fever : immunohistochemical and ultrastructural study of accumulated tubulin-immunoreactive material

Acta neuropathologica, 1992, Vol.83 (4), p.440-444

1992

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PMP-22 gene duplications and deletions identified in archival, paraffin-embedded sural nerve biopsy specimens : correlation to structural changes

Acta neuropathologica, 1998-07, Vol.96 (1), p.13-21

1998

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Spasmodic torticollis : severe compression neuropathy in rami dorsales of cervical nerves C1-6

Acta neuropathologica, 1992-09, Vol.84 (4), p.416-424

1992

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Myenteric plexus neuropathy in infantile hypertrophic pyloric stenosis

Acta neuropathologica, 1989-01, Vol.78 (6), p.649-661

1989

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Mitochondrial abnormalities and intrafamilial variability of sural nerve biopsy findings in adrenomyeloneuropathy

Acta neuropathologica, 1996-07, Vol.92 (1), p.64-69

1996

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Peripheral nerve and skeletal muscle involvement in CADASIL

X-linked dominant Charcot-Marie-Tooth disease : nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)

Morphological changes following experimental intraventricular haemorrhage and intraventricular fibrinolytic treatment with recombinant tissue plasminogen activator

Comparative morphometric evaluation of peripheral nerves and muscle fibers in myotonic dystrophy

Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency

Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Major histocompatibility complex class II expression by activated microglia caudal to lesions of descending tracts in the human spinal cord is not associated with a T cell response

Demyelinating sensorimotor neuropathy with congenital cataract, mental retardation, and unique, dysplastic perineurial cells within the endoneurium

Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis)

Screening for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsy in archival nerve biopsy samples by direct-double-differential PCR

Polyneuropathy with osmiophilic membrane-bound, cytoplasmic inclusions in Schwann cells (POMCIS)

Changes of the ratio between myelin thickness and axon diameter in human developing sural, femoral, ulnar, facial, and trochlear nerves

Dominantly inherited myopathy with novel tubular aggregates containing 1-21 tubulofilamentous structures

Inhibitory effects of thalidomide on cellular proliferation, endoneurial edema and myelin phagocytosis during early Wallerian degeneration

Nuclear and mitochondrial changes of muscle fibers in AIDS after treatment with high doses of zidovudine

Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions

Fine structural evaluation of altered Schmidt-Lanterman incisures in human sural nerve biopsies

Significance of degenerating endoneurial cells in peripheral neuropathy

Correlation between the number of epineurial and endoneurial blood vessels in diseased human sural nerves

Colchicine myopathy in a case of familial mediterranean fever : immunohistochemical and ultrastructural study of accumulated tubulin-immunoreactive material

PMP-22 gene duplications and deletions identified in archival, paraffin-embedded sural nerve biopsy specimens : correlation to structural changes

Spasmodic torticollis : severe compression neuropathy in rami dorsales of cervical nerves C1-6

Myenteric plexus neuropathy in infantile hypertrophic pyloric stenosis

Mitochondrial abnormalities and intrafamilial variability of sural nerve biopsy findings in adrenomyeloneuropathy

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