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You searched for: Author/Creator Clementi, Maurizio

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1. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Issue 1 (December 2016)

2. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Issue 1 (December 2016)

4. Advances in the Pathogenesis of Cardiorenal Syndrome Type 3. (4th March 2015)

5. Advances in the Pathogenesis of Cardiorenal Syndrome Type 3. (4th March 2015)

6. Advising Mothers on the Use of Medications during Breastfeeding: A Need for a Positive Attitude. (February 2016)

7. Catechol‐O‐Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta‐Analysis of Previously Published Studies. (22nd October 2017)

9. Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1. Issue 1 (26th October 2019)

10. Correlation of peripapillary retinal nerve fibre layer thickness with visual acuity in paediatric patients affected by optic pathway glioma. Issue 8 (3rd October 2018)