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Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?

Neuromuscular disorders : NMD, 2011-04, Vol.21 (4), p.263-271

Fitzsimons, Robin B

2011

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Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

Annals of neurology, 2001-06, Vol.49 (6), p.753-760

2001

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Facioscapulohumeral muscular dystrophy

Current opinion in neurology, 1999-10, Vol.12 (5), p.501-511

Fitzsimons, R B

1999

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Gustav Nossal wends his way to WHO

The Lancet (British edition), 1996-07, Vol.348 (9019), p.54-54

Fitzsimons, Robin

1996

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Neural control of the sequence of expression of myosin heavy chain isoforms in foetal mammalian muscles

Development (Cambridge), 1989-12, Vol.107 (4), p.751-769

1989

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Facioscapulohumeral dystrophy: The role of inflammation

The Lancet (British edition), 1994-10, Vol.344 (8927), p.902

Fitzsimons, Robin B

1994

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Facioscapulohumeral dystrophy: the role of inflammation

The Lancet (British edition), 1994-10, Vol.344 (8927), p.902-903

Fitzsimons, RobinB

1994

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Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy: a general association with genetic and therapeutic implications

Brain (London, England : 1878), 1987-06, Vol.110 (3), p.631-648

1987

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Primary, secondary and tertiary myotubes in developing skeletal muscle: A new approach to the analysis of human myogenesis

Journal of the neurological sciences, 1987-10, Vol.81 (1), p.19-43

1987

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RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY

Brain (London, England : 1878), 1987-06, Vol.110 (3), p.631-648

1987

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Migraine coma: meningitic migraine with cerebral œdema associated with a new form of autosomal dominant cerebellar ataxia

Brain (London, England : 1878), 1985-09, Vol.108 (3), p.555-577

1985

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Myosin heavy chain composition of single fibres and their origins and distribution in developing fascicles of sheep tibialis cranialis muscles

Journal of muscle research and cell motility, 1992-10, Vol.13 (5), p.551-572

1992

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The Fifth International Congress on Neuromuscular Diseases, Marseilles, France, September, 1982

Journal of muscle research and cell motility, 1983-02, Vol.4 (1), p.3-4

Fitzsimons, Robin

1983

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Whose law will rule Hong Kong?

Times (London, England : 1788), 1993-06, p.37-37

Fitzsimons, Robin

1993

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Embryonic and foetal myosins in human skeletal muscle: The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy

Journal of the neurological sciences, 1981-01, Vol.52 (2), p.367-384

1981

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MIGRAINE COMA

Brain (London, England : 1878), 1985-09, Vol.108 (3), p.555-577

1985

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A study of a myopathy presenting as idiopathic scoliosis

Journal of the neurological sciences, 1980-04, Vol.46 (1), p.33-48

1980

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Ultrastructural identification of type 1 fibres in human skeletal muscle

Journal of the neurological sciences, 1988-01, Vol.83 (1), p.93-108

1988

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Ultrastructural identification of type 1 fibres in human skeletal muscle: Immunogold labelling of thin cryosections with a monoclonal antibody against slow myosin

Journal of the neurological sciences, 1988, Vol.83 (1), p.93-108

1988

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FETAL MYOSINS IN SKELETAL MUSCLE FROM A PATIENT WITH MYALGIA AND FATIGUE

The Lancet (British edition), 1982-02, Vol.319 (8270), p.480-483

1982

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Embryonic and foetal myosins in human skeletal muscle

Journal of the neurological sciences, 1981-11, Vol.52 (2-3), p.367-384

1981

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Myopathy with pathological features of both centronuclear myopathy and multicore disease

Journal of the Neurological Sciences, 1982-12, Vol.57 (2), p.395-405

1982

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A study of a myopathy presenting as idiopathic scoliosis: Multicore disease or mitochondrial myopathy?

Journal of the neurological sciences, 1980-01, Vol.46 (1), p.33-48

1980

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Fungal retinitis: a case of Torulopsis glabrata infection treated with miconazole

British journal of ophthalmology, 1980-09, Vol.64 (9), p.672-675

1980

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New techniques for the ultrastructural identification of human skeletal muscle fibre types

Cell biology international reports, 1987-03, Vol.11 (3), p.247-247

1987

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Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?

Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

Facioscapulohumeral muscular dystrophy

Gustav Nossal wends his way to WHO

Neural control of the sequence of expression of myosin heavy chain isoforms in foetal mammalian muscles

Facioscapulohumeral dystrophy: The role of inflammation

Facioscapulohumeral dystrophy: the role of inflammation

Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy: a general association with genetic and therapeutic implications

Primary, secondary and tertiary myotubes in developing skeletal muscle: A new approach to the analysis of human myogenesis

RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY

Migraine coma: meningitic migraine with cerebral œdema associated with a new form of autosomal dominant cerebellar ataxia

Myosin heavy chain composition of single fibres and their origins and distribution in developing fascicles of sheep tibialis cranialis muscles

The Fifth International Congress on Neuromuscular Diseases, Marseilles, France, September, 1982

Whose law will rule Hong Kong?

Embryonic and foetal myosins in human skeletal muscle: The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy

MIGRAINE COMA

A study of a myopathy presenting as idiopathic scoliosis

Ultrastructural identification of type 1 fibres in human skeletal muscle

Ultrastructural identification of type 1 fibres in human skeletal muscle: Immunogold labelling of thin cryosections with a monoclonal antibody against slow myosin

FETAL MYOSINS IN SKELETAL MUSCLE FROM A PATIENT WITH MYALGIA AND FATIGUE

Embryonic and foetal myosins in human skeletal muscle

Myopathy with pathological features of both centronuclear myopathy and multicore disease

A study of a myopathy presenting as idiopathic scoliosis: Multicore disease or mitochondrial myopathy?

Fungal retinitis: a case of Torulopsis glabrata infection treated with miconazole

New techniques for the ultrastructural identification of human skeletal muscle fibre types

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