IRIS
ACCOGLI, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 40
Totale 40
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Nazione #
IT - Italia 40
Totale 40
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Città #
Genoa 17
Genova 14
Rapallo 5
Bordighera 4
Totale 40
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Nome #
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome, file e268c4cd-d4c5-a6b7-e053-3a05fe0adea1 11
An eleven-year history of Vanishing White Matter Disease in an adult patient with no cognitive decline and EIF2B5 mutations. A case report, file a37652d2-283f-477e-9f51-817212b2f1f3 7
A rare triad of morning glory disc anomaly, moyamoya vasculopathy, and transsphenoidal cephalocele: pathophysiological considerations and surgical management, file e268c4ce-08eb-a6b7-e053-3a05fe0adea1 4
Musculoskeletal features without ataxia associated with a novel de novo mutation in KCNA1 impairing the voltage sensitivity of Kv1.1 channel, file e268c4cd-d997-a6b7-e053-3a05fe0adea1 3
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development, file e268c4cb-f334-a6b7-e053-3a05fe0adea1 2
Idiopathic Cervical Hematomyelia in an Infant: Spinal Cord Injury without Radiographic Abnormality Caused by a Trivial Trauma? Case Report and Review of the Literature, file e268c4cc-0a83-a6b7-e053-3a05fe0adea1 2
Chiari malformation type I: what information from the genetics?, file e268c4cc-1268-a6b7-e053-3a05fe0adea1 2
Biallelic Variants in KIF17 Associated with Microphthalmia and Coloboma Spectrum, file 9c4c05a9-420f-44fc-bbb9-d921a5962948 1
A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions, file e268c4cb-9411-a6b7-e053-3a05fe0adea1 1
Novel CNS malformations and skeletal anomalies in a patient with Beaulieu-boycott-Innes syndrome, file e268c4cb-941c-a6b7-e053-3a05fe0adea1 1
Familial ROBO1 deletion associated with ectopic posterior pituitary, duplication of the pituitary stalk and anterior pituitary hypoplasia, file e268c4cb-95e1-a6b7-e053-3a05fe0adea1 1
Surgical results of cranioplasty with a polymethylmethacrylate customized cranial implant in pediatric patients: A single-center experience, file e268c4cc-0a77-a6b7-e053-3a05fe0adea1 1
Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition?, file e268c4cc-0c27-a6b7-e053-3a05fe0adea1 1
Genetic Screening of Pediatric Cavernous Malformations, file e268c4cc-2ef6-a6b7-e053-3a05fe0adea1 1
NovelAMPD2mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities, file e268c4cc-4895-a6b7-e053-3a05fe0adea1 1
CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations, file e268c4cd-0121-a6b7-e053-3a05fe0adea1 1
Totale 40
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Categoria #
all - tutte 227
article - articoli 227
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 454
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203 0 0 0 0 0 0 0 1 1 1 0 0
2020/20217 0 0 1 0 0 0 0 4 0 1 1 0
2021/20224 0 1 1 0 0 0 0 0 2 0 0 0
2022/20238 0 0 0 0 0 0 4 0 0 0 3 1
2023/202418 0 0 1 5 0 1 5 4 1 1 0 0
Totale 40