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Collection : Aix-Marseille Universite

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Academic Journal

Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders

Authors : Schluth-Bolard, Caroline, Schluth; Diguet, Flavie; Chatron, Nicolas ...

Subjects: intellectual disability; chromosomal rearrangements; whole genome sequencing

Source: ISSN: 0022-2593.

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Academic Journal

Movement disorders in patients with alternating hemiplegia ; Movement disorders in patients with alternating hemiplegia: 'Soft' and 'stiff' at the same time

Authors : Panagiotakaki, Eleni; Doummar, Diane; Nogué, Erika ...

Subjects: dystonia; chorea; developmental disorders

Source: ISSN: 0028-3878.

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Academic Journal

Early movement restriction leads to maladaptive plasticity in the sensorimotor cortex and to movement disorders

Authors : Delcour, Maxime, S; Russier, Michaël; Castets, Francis ...

Subjects: Developmental disorders; Neurodevelopmental disorders; [SDV]Life Sciences [q-bio]

Source: ISSN: 2045-2322.

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Academic Journal

Early movement restriction leads to maladaptive plasticity in the sensorimotor cortex and to movement disorders

Authors : Delcour, Maxime; Russier, Michaël; Castets, Francis ...

Subjects: Developmental disorders; Neurodevelopmental disorders; [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology

Source: ISSN: 2045-2322.

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Academic Journal

The Glasgow Voice Memory Test: assessing the ability to memorize and recognize unfamiliar voices

Authors : Aglieri, Virginia; Watson, Rebecca; Pernet, Cyril ...

Subjects: Voice recognition; Phonagnosia; Individual differences

Source: ISSN: 1554-351X.

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Academic Journal

Le devenir à l'adolescence d'enfants atteints de troubles envahissants du développement : l'exemple de l'hôpital de jour d'Aix-en-Provence.

Authors : Carbonnel Chabas, Claire; Gepner, Bruno;

Subjects: Autisme; Troubles envahissants du développement; Devenir

Source: ISSN: 0222-9617 ; Neuropsychiatrie de l'Enfance et de l'Adolescence ; https://hal.science/hal-00484205 ; Neuropsychiatrie de l'Enfance et de l'Adolescence, 2009, 57, pp.118-127.

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Academic Journal

Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

Authors : Morsy, Heba; Benkirane, Mehdi; Cali, Elisa ...

Subjects: Developmental delay; Developmental epileptic encephalopathy; Hereditary ataxia

Source: ISSN: 1098-3600.

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Academic Journal

Structural gray matter features and behavioral preliterate skills predict future literacy – A machine learning approach

Authors : Beyer, Moana; Liebig, Johanna; Sylvester, Teresa ...

Subjects: MRI; machine learning; reading acquisition

Source: ISSN: 1662-4548.

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Academic Journal

MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects

Authors : Coursimault, Juliette; Guerrot, Anne-Marie; Morrow, Michelle ...

Subjects: MESH: Adolescent; MESH: Adult; MESH: Obesity

Source: ISSN: 0340-6717.

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Academic Journal

Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans

Authors : Le, Thuy-Linh; Galmiche, Louise; de Coo, Irenaeus, F M ...

Subjects: [SDV]Life Sciences [q-bio]

Source: ISSN: 0021-9738 ; Journal of Clinical Investigation ; https://amu.hal.science/hal-03173467 ; Journal of Clinical Investigation, 2021, 131 (6), ⟨10.1172/jci145837⟩.

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