Luigi Tarani | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Fetal alcohol spectrum disorders awareness in health professionals: Implications for psychiatry	RIVISTA DI PSICHIATRIA	2020
Neuroinflammatory markers in the serum of prepubertal children with down syndrome	JOURNAL OF IMMUNOLOGY RESEARCH	2020
From mini-puberty to pre-puberty: early impairment of the hypothalamus–pituitary–gonadal axis with normal testicular function in children with non-mosaic Klinefelter syndrome	JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION	2020
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases	THE ITALIAN JOURNAL OF PEDIATRICS	2020
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence)	ORPHANET JOURNAL OF RARE DISEASES	2020
PNPLA3 gene polymorphism is associated with liver steatosis in children with Down syndrome	NMCD. NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES	2020
The dark side of COVID-19: The need of integrated medicine for children with special care needs	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2020
Mowat-Wilson syndrome: growth charts	ORPHANET JOURNAL OF RARE DISEASES	2020
Klinefelter’s Syndrome, From a Disabling Condition to a Variant of Normalcy	Klinefelter’s Syndrome, From a Disabling Condition to a Variant of Normalcy	2020
Reasoning on figurative language: A preliminary study on children with autism spectrum disorder and klinefelter syndrome	BRAIN SCIENCES	2019
High-level language competencies and Theory of Mind in a group of children with Klinefelter syndrome	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2019
Beyond the literal meaning of words in children with klinefelter syndrome: two case studies	BRAIN SCIENCES	2018
Fetal alcohol spectrum disorders in pediatrics FASD and the pediatrician	BIOMEDICAL REVIEWS	2018
Nerve growth factor in brain diseases	BIOMEDICAL REVIEWS	2018
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care	GENETICS IN MEDICINE	2018
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients	GENETICS IN MEDICINE	2017
Unreliable estimation of prevalence of fetal alcohol syndrome	THE LANCET GLOBAL HEALTH	2017
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion. Potential role of PI3K/Akt pathway dysregulation	EUROPEAN JOURNAL OF MEDICAL GENETICS	2017
FOXP1-related intellectual disability syndrome: a recognisable entity	EJMG	2017
TMJ replacement utilizing patient-fitted TMJ TJR devices in a re-ankylosis child	JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY	2016