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NOZZA P

Last name: NOZZA P

2018 (v1)

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Medico-legal investigation in an explicable case of congenital central hypoventilation syndrome due to a rare variant of the PHOX2B gene

Ventura F Barranco R Bachetti T

The heterozygous PHOX2B gene mutation is related to congenital central hypoventilation syndrome (CCHS). It is characterized by defective autonomous nervous system development leading to inadequate breathing response to hypoxia and hypercapnia, leading to hypoventilation especially during non-REM sleep, but also during waking in the more severe...

Uploaded on: April 14, 2023
2012 (v1)

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A 3-year-old boy with drug-resistant complex partial seizures

STRIANO, PASQUALE BAGLIETTO, MARIA GIUSEPPINA Consales A

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Uploaded on: March 31, 2023
2013 (v1)

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Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomy.

Consales A Nozza P Ravegnani M

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Uploaded on: April 14, 2023
2009 (v1)

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Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective.

Garrè ML Cama A Bagnasco F

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Uploaded on: May 11, 2023