N. Cavanagh

发表

Intracranial calcification in paediatric computed tomography

B. Kendall, N. Cavanagh, 2004, Neuroradiology.

Calf hypertrophy and asymmetry in female carriers of X‐linked Duchenne muscular dystrophy: an over‐diagnosed clinical manifestation

N. Cavanagh, M. A. Pkeece, 1981, Clinical genetics.

Clinical clues to progressive degenerative disorders of the central nervous system.

N. Cavanagh, 1983, Journal of tropical pediatrics.

Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers.

F. Howard, N. Cavanagh, J. Bicknell, 1974, Archives of disease in childhood.

High Density on Computed Tomography in Infantile Krabbe's Disease: a Case Report

B. Kendall, N. Cavanagh, 1986, Developmental medicine and child neurology.

Neurological aspects of biopterin metabolism.

K. Hyland, R. Leeming, I. Smith, 1986, Archives of disease in childhood.

Hereditary sensory neuropathy with spastic paraplegia.

R. Galvin, R. Eames, N. Cavanagh, 1979, Brain : a journal of neurology.

Psoriasis, psoriatic arthropathy and relapsing orbital myositis

N. Cavanagh, S. Mayou, R. Ajitsaria, 2001, Clinical and experimental dermatology.

Letter: Hydrocephalus treated by compressive head wrapping.

E. Boltshauser, N. Cavanagh, 1976, Archives of disease in childhood.

Alternating hemiplegia: complicated migraine of infancy.

G. Hosking, J. Wilson, N. Cavanagh, 1978, Archives of disease in childhood.

Possible manifestation of the dystrophic X chromosome in muscle cultures from carriers of Duchenne muscular dystrophy

E. Thompson, B. Lake, R. Yasin, 1983, Experimental Neurology.

Creatine kinase isoenzymes in cultured human muscle cells. I. Comparison of Duchenne muscular dystrophy with other myopathic and neurogenic disease.

E. Thompson, R. Yasin, N. Cavanagh, 1981, Clinica chimica acta; international journal of clinical chemistry.

Shwachman's syndrome. A review of 21 cases.

P. Aggett, D. Matthew, J. Harries, 1980, Archives of disease in childhood.

THE RÔLE OF THYMECTOMY IN CHILDHOOD MYASTHENIA

N. Cavanagh, 1980, Developmental medicine and child neurology.

Mucocele of the paranasal sinuses as a cause of orbital hypertelorism

I. Jackson, N. Cavanagh, J. Lehman, 1987, European Journal of Plastic Surgery.

Metachromatic leucodystrophy: review of 38 cases.

R. Macfaul, B. Lake, R. Stephens, 1982, Archives of disease in childhood.

Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook.

B. Lake, N. Cavanagh, P. McMeniman, 1979, Archives of disease in childhood.

MYOPATHY WITH MINICORES IN SIBLINGS

J. Wilson, N. Cavanagh, B. Lake, 1977 .

Early-juvenile Batten's disease — A recognisable sub-group distinct from other forms of Batten's disease Analysis of 5 patients

B. Lake, N. Cavanagh, 1978, Journal of the Neurological Sciences.

Neurotoxicity in lymphoblastic leukaemia: comparison of oral and intramuscular methotrexate and two doses of radiation.

L. Jannoun, B. Kendall, S. Richards, 1990, Archives of disease in childhood.

Outcome in congenital stridor (laryngomalacia).

N. Cavanagh, P. McSwiney, P. Languth, 1977, Archives of disease in childhood.

ORAL TREATMENT OF CARNITINE MYOPATHY

J. Wilson, G. Hosking, N. Cavanagh, 1977, The Lancet.

Thenar hypoplasia with associated radiologic abnormalities

D. Yates, N. Cavanagh, J. Sutcliffe, 1979, Muscle & nerve.

Child with weak muscles: Recognition, causes and management

N. Cavanagh, 1996 .

Ring 20 chromosome in a child with seizures, minor anomalies, and retardation.

D. Hughes, N. Cavanagh, J. Stewart, 1979, Archives of disease in childhood.

Ulnar nerve tumours of the hand in childhood

J. Pincott, N. Cavanagh, 1977, Journal of neurology, neurosurgery, and psychiatry.

HERPES-SIMPLEX INFECTION PRESENTING AS BRAINSTEM ENCEPHALITIS

J. Wilson, T. Fenton, N. Cavanagh, 1977, The Lancet.

Patterns of intellectual change in the dementing school child.

N. Cavanagh, M. Lobascher, 1980, Child: care, health and development.

The other handicap: brightness.

N. Cavanagh, M. Lobascher, 1977, British medical journal.

THE POSSIBLE ADJUVANT ROLE OF BORDETELLA PERTUSSIS AND PERTUSSIS VACCINE IN CAUSING SEVERE ENCEPHALOPATHIC ILLNESS: A PRESENTATION OF THREE CASE HISTORIES

E. Brett, J. Wilson, N. Cavanagh, 1981, Neuropediatrics.

The role of transferrin saturation as a screening test for hereditary haemochromatosis in an Irish population seeking medical care

N. Cavanagh, R. O'hara, M. Cullina, 2003, Annals of clinical biochemistry.

Creatine kinase isoenzymes in cultured human muscle cells. II. A study of carrier females for Duchenne muscular dystrophy by needle and open biopsy.

E. Thompson, R. Yasin, N. Cavanagh, 1981, Clinica chimica acta; international journal of clinical chemistry.