Willshaw H - Search Results

1

Guidelines for the diagnosis and management of individuals with neurofibromatosis 1.

Ferner RE, Huson SM, Thomas N, Moss C, Willshaw H, Evans DG, Upadhyaya M, Towers R, Gleeson M, Steiger C, Kirby A. Ferner RE, et al. Among authors: willshaw h. J Med Genet. 2007 Feb;44(2):81-8. doi: 10.1136/jmg.2006.045906. Epub 2006 Nov 14. J Med Genet. 2007. PMID: 17105749 Free PMC article. Review.

2

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

Glass IA, Good P, Coleman MP, Fullwood P, Giles MG, Lindsay S, Nemeth AH, Davies KE, Willshaw HA, Fielder A, et al. Glass IA, et al. Among authors: willshaw ha. J Med Genet. 1993 Dec;30(12):1044-50. doi: 10.1136/jmg.30.12.1044. J Med Genet. 1993. PMID: 7907666 Free PMC article.

3

Septo-optic dysplasia: antenatal risk factors and clinical features in a regional study.

Atapattu N, Ainsworth J, Willshaw H, Parulekar M, MacPherson L, Miller C, Davies P, Kirk JM. Atapattu N, et al. Among authors: willshaw h. Horm Res Paediatr. 2012;78(2):81-7. doi: 10.1159/000341148. Epub 2012 Aug 14. Horm Res Paediatr. 2012. PMID: 22907285 Clinical Trial.

4

Incidence and patterns of detection and management of childhood-onset hereditary retinal disorders in the UK.

Hamblion EL, Moore AT, Rahi JS; British Childhood Onset Hereditary Retinal Disorders Network. Hamblion EL, et al. Br J Ophthalmol. 2012 Mar;96(3):360-5. doi: 10.1136/bjo.2010.201178. Epub 2011 Jun 7. Br J Ophthalmol. 2012. PMID: 21653210

5

Improving detection of blindness in childhood: the British Childhood Vision Impairment study.

Rahi JS, Cumberland PM, Peckham CS; British Childhood Visual Impairment Interest Group. Rahi JS, et al. Pediatrics. 2010 Oct;126(4):e895-903. doi: 10.1542/peds.2010-0498. Epub 2010 Sep 20. Pediatrics. 2010. PMID: 20855395

6

Relationship of infantile periocular hemangioma depth to growth and regression pattern.

Tambe K, Munshi V, Dewsbery C, Ainsworth JR, Willshaw H, Parulekar MV. Tambe K, et al. Among authors: willshaw h. J AAPOS. 2009 Dec;13(6):567-70. doi: 10.1016/j.jaapos.2009.09.014. J AAPOS. 2009. PMID: 20006818

7

Subinternal limiting membrane hemorrhage with perimacular fold in leukemia.

Bhatnagar A, Wilkinson LB, Tyagi AK, Willshaw HE. Bhatnagar A, et al. Among authors: willshaw he. Arch Ophthalmol. 2009 Nov;127(11):1548-50. doi: 10.1001/archophthalmol.2009.284. Arch Ophthalmol. 2009. PMID: 19901230 No abstract available.

8

Paediatric blepharoptosis: a 10-year review.

Berry-Brincat A, Willshaw H. Berry-Brincat A, et al. Among authors: willshaw h. Eye (Lond). 2009 Jul;23(7):1554-9. doi: 10.1038/eye.2008.311. Epub 2008 Oct 24. Eye (Lond). 2009. PMID: 18949007

9

Visual loss and idiopathic intracranial hypertension in children with Alagille syndrome.

Narula P, Gifford J, Steggall MA, Lloyd C, Van Mourik ID, Mckiernan PJ, Willshaw HE, Kelly D. Narula P, et al. Among authors: willshaw he. J Pediatr Gastroenterol Nutr. 2006 Sep;43(3):348-52. doi: 10.1097/01.mpg.0000221895.51748.44. J Pediatr Gastroenterol Nutr. 2006. PMID: 16954958

10

Neurodevelopmental implications of ocular motor apraxia.

Marr JE, Green SH, Willshaw HE. Marr JE, et al. Among authors: willshaw he. Dev Med Child Neurol. 2005 Dec;47(12):815-9. doi: 10.1017/S0012162205001726. Dev Med Child Neurol. 2005. PMID: 16288671 Free article.

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