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Donatella Milani

Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico di Milano
H指数:36
被引数:4,617

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Beyond Rett syndrome: a case series expanding the neurological spectrum associated with pathogenic MECP2 variants

超越雷特综合征:扩展与致病性MECP2变异相关神经谱系的一个病例系列

2026-08-260
PRE
International Clinical Evidence-based Guideline for Kleefstra Syndrome
2026-01-200
OAAI
Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies—30 Years' Experience From a Third Level Center

《一个谱系的面貌:一个大宗染色质病队列的临床与遗传特征分析——来自一家三级医疗中心30年的经验》

2025-11-020
OAAI
Beckwith-Wiedemann spectrum (BWSp): an update on diagnosis, management, and follow-up from the scientific committee of the Italian BWSp association

贝克威思-威德曼谱系 (BWSp):意大利BWSp协会科学委员会关于诊断、管理和随访的最新进展

2025-10-240
OAAI
Genetic variants and phenotypic data curated for the CAGI6 intellectual disability panel challenge
2025-02-280
OAAI
A long way to syndromic short stature

综合征性身材矮小的漫长道路

2024-09-270
OAAI
Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement
2024-03-1212
OAAI
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods

CAGI,基因组解释的关键评估,建立了计算遗传变异解释方法的进展和前景

2024-02-2210
OAAI
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes
BRAIN
IF11.7
2023-12-012
OA
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss

短生长期毛发综合征: 与WNT10A中的单等位基因和双等位基因变体以及与男性脱发的遗传重叠有关

2023-09-063
OA
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology

CUX1-related神经发育障碍: 深入了解表型-基因型谱和潜在病理

2023-08-305
OAAI