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1. Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis

2. Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders

4. Sex, gender, and retinoblastoma: analysis of 4351 patients from 153 countries

5. Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

8. The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries

10. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

11. Intra-arterial chemotherapy for retinoblastoma in Australia: 11-year experience

13. Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucoma

15. Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

16. Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort

17. Pathogenic genetic variants identified in Australian families with paediatric cataract

20. Optical treatment of amblyopia in older children and adults is essential prior to enrolment in a clinical trial

21. Effectiveness of a Binocular Video Game vs Placebo Video Game for Improving Visual Functions in Older Children, Teenagers, and Adults With Amblyopia: A Randomized Clinical Trial

23. Danish heritable retinoblastoma survivors' perspectives on reproductive choices: "It's important for me, not to pass on this condition".

24. Defining High-risk Retinoblastoma

25. Establishing risk of vision loss in Leber hereditary optic neuropathy

26. Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry

27. Sex, gender, and retinoblastoma: analysis of 4351 patients from 153 countries

32. Adherence to home-based videogame treatment for amblyopia in children and adults

40. Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma

41. Adherence to home-based videogame treatment for amblyopia in children and adults

42. The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohort

43. The genetic and clinical landscape of nanophthalmos in an Australian cohort

48. Prevalence ofFOXC1Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma

49. CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma

50. Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders

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