Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("HARBORD, M")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 21 of 21

  • Page / 1
Export

Selection :

  • and

Significant anticonvulsant side-effects in children and adolescentsHARBORD, M. G.Journal of clinical neuroscience. 2000, Vol 7, Num 3, pp 213-216, issn 0967-5868Article

Levodopa responsive Parkinsonism in adults with Angelman SyndromeHARBORD, M.Journal of clinical neuroscience. 2001, Vol 8, Num 5, pp 421-422, issn 0967-5868Conference Paper

Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophyMENEZES, M. P; WADDELL, L. B; HARBORD, M et al.Neurology. 2012, Vol 78, Num 16, pp 1258-1263, issn 0028-3878, 6 p.Article

Correlation between the immune responses to collagens type I, III, IV and V and Klebsiella pneumoniae in patients with Crohn's disease and ankylosing spondylitisTIWANA, H; NATT, R. S; BENITEZ-BRITO, R et al.Rheumatology (Oxford. Print). 2001, Vol 40, Num 1, pp 15-23, issn 1462-0324Article

The effect of cisapride on dyspepsia symptoms and the electrogastrogram in patients with non-ulcer dyspepsiaBESHERDAS, K; LEAHY, A; MASON, I et al.Alimentary pharmacology & therapeutics. 1998, Vol 12, Num 8, pp 755-759, issn 0269-2813Article

Anti-tumour necrosis factor-α therapy for severe enteropathy in patients with common variable immunodeficiency (CVID)CHUA, I; STANDISH, R; LEAR, S et al.Clinical and experimental immunology (Print). 2007, Vol 150, Num 2, pp 306-311, issn 0009-9104, 6 p.Article

Bilateral occipital calcification associated with celiac disease, folate deficiency, and epilepsyLEA, M. E; HARBORD, M; SAGE, M. R et al.American journal of neuroradiology. 1995, Vol 16, Num 7, pp 1498-1500, issn 0195-6108Article

In-depth analysis of delays to patient discharge: a metropolitan teaching hospital experienceHENDY, P; PATEL, J. H; KORDBACHEH, T et al.Clinical medicine. 2012, Vol 12, Num 4, pp 320-323, issn 1470-2118, 4 p.Article

Subacute sclerosing panencephalitis presenting as schizophreniform psychosisDUNCALF, C. M; KENT, J. N. G; HARBORD, M et al.British journal of psychiatry (Print). 1989, Vol 155, pp 557-559, issn 0007-1250, SUP6Article

Alexander's disease: cranial ultrasound findingsHARBORD, M. G; LEQUESNE, G. W.Pediatric radiology. 1988, Vol 18, Num 3, pp 227-228, issn 0301-0449Article

Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndromeHARBORD, M. G; BARAITSER, M; WILSON, J et al.Journal of medical genetics. 1989, Vol 26, Num 6, pp 397-400, issn 0022-2593, 4 p.Article

Infant onset subacute necrotizing encephalomyelopathy (Leigh's disease)MORRIS, S. A; HARBORD, M. G.Journal of paediatrics and child health. 1993, Vol 29, Num 5, pp 363-367, issn 1034-4810Article

Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblingsHARBORD, M. G; HARDEN, A; HARDING, B et al.Neuropediatrics. 1990, Vol 21, Num 3, pp 164-168, issn 0174-304X, 5 p.Article

Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblingsHARBORD, M. G; HALL-GRAGGS, M. A; KENDALL, B et al.Neuropediatrics. 1990, Vol 21, Num 4, pp 218-221, issn 0174-304X, 4 p.Article

Benign familial disease with muscle mounding and ripplingBURNS, R. J; BRETAG, A. H; BLUMBERGS, P. C et al.Journal of neurology, neurosurgery and psychiatry. 1994, Vol 57, Num 3, pp 344-347, issn 0022-3050Conference Paper

Impaired neutrophil chemotaxis in Crohn's disease relates to reduced production of chemokines and can be augmented by granulocyte-colony stimulating factorHARBORD, M. W. N; MARKS, D. J. B; FORBES, A et al.Alimentary pharmacology & therapeutics. 2006, Vol 24, Num 4, pp 651-660, issn 0269-2813, 10 p.Article

Autosomal recessive microcephaly, mental retardation with non pigmentary retinopathy and a distinctive electroretinogramHARBORD, M. G; LAMBERT, S. R; KRIS, A et al.Neuropediatrics. 1989, Vol 20, Num 3, pp 139-141, issn 0174-304XArticle

Moebius' syndrome with unilateral cerebellar hypoplasiaHARBORD, M. G; FINN, J. P; HALL-CRAGGS, M. A et al.Journal of medical genetics. 1989, Vol 26, Num 9, pp 579-582, issn 0022-2593Article

Central nervous system malformations in Mohr's syndromeREARDON, W; HARBORD, M. G; HALL-CRAGGS, M. A et al.Journal of medical genetics. 1989, Vol 26, Num 10, pp 659-663, issn 0022-2593Article

Aicardi syndrome : MR assessment of brain structure and myelinationHALL-CRAGGS, M. A; HARBORD, M. G; FINN, J. P et al.American journal of neuroradiology. 1990, Vol 11, Num 3, pp 532-536, issn 0195-6108, 5 p.Article

Early onset leukodystrophy with distinct facial features in 2 siblingsHARBORD, M. G; FINN, J. P; HALL-GRAGGS, M. A et al.Neuropediatrics. 1989, Vol 20, Num 3, pp 154-157, issn 0174-304XArticle

  • Page / 1