A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 3, p. 276, doi. 10.1111/cge.12277
- By:
- Publication type:
- Article
Works matching AU Dali C
Results: 5
1
2
Cognitive profile and activities of daily living: 35 patients with alpha-mannosidosis.
- Published in:
- Journal of Inherited Metabolic Disease, 2015, v. 38, n. 6, p. 1119, doi. 10.1007/s10545-015-9862-4
- By:
- Publication type:
- Article
3
Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study.
- Published in:
- Journal of Inherited Metabolic Disease, 2013, v. 36, n. 6, p. 1015, doi. 10.1007/s10545-013-9595-1
- By:
- Publication type:
- Article
4
Combined surgical treatment of symptomatic carotid, coronary and mesenteric occlusive disease.
- Published in:
- Journal of Surgical Case Reports, 2020, v. 2020, n. 2, p. N.PAG, doi. 10.1093/jscr/rjz392
- By:
- Publication type:
- Article
5
Threshold electrical stimulation (TES) in ambulant children with CP: a randomized double-blind placebo-controlled clinical trial.
- Published in:
- 2002
- By:
- Publication type:
- journal article