Annalisa Calcagno
Genoa, 16147, Italy
Last Updated: 09/26/2026
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Found 14 publications
Development of Functional Abilities Assessment in Paediatric Oncology (FAAP-O) Scale for Children and Adolescents Affected by Cancer.
Journal: Children (Basel, Switzerland)
Published: July 29, 2025
Enhancement of postural control and upper limb function following selective dorsal rhizotomy: a retrospectively registered study.
Journal: European journal of pediatrics
Published: May 30, 2025
Five-Year Retrospective Cohort Study of Changes in the International Classification of Functioning, Disability and Health of Children and Youth Parameters in Cerebral Palsy Children and Adolescents With Continuous Intrathecal Baclofen Therapy Versus Control Group.
Journal: American journal of physical medicine & rehabilitation
Published: November 13, 2024
Internal Consistency and Floor/Ceiling Effects of the Gross Motor Function Measure for Use with Children Affected by Cancer: A Cross-Sectional Study.
Journal: Current oncology (Toronto, Ont.)
Published: June 28, 2024
'Distal 16p12.2 microdeletion' in a patient with autosomal recessive deafness-22.
Journal: Journal of genetics
Published: June 18, 2019
Novel CNS malformations and skeletal anomalies in a patient with Beaulieu-boycott-Innes syndrome.
Journal: American journal of medical genetics. Part A
Published: April 03, 2018
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases.
Journal: European journal of endocrinology
Published: February 02, 2018
CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations.
Journal: European journal of medical genetics
Published: January 18, 2018
Classical and non-classical causes of GH deficiency in the paediatric age.
Journal: Best practice & research. Clinical endocrinology & metabolism
Published: December 16, 2016
Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Journal: Clinical epigenetics
Published: April 07, 2016
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Journal: Clinical epigenetics
Published: July 27, 2015
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.
Journal: European journal of endocrinology
Published: March 06, 2015
Last Updated: 09/26/2026