Search Results - "Neurodevelopmental disorder"

Schizophrenia Evolution and Synthesis

Subjects: “…neurodevelopmental disorder…”
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Epilepsy

Subjects: “…Pathology of Epilepsy; Anatomical Basis of Seizures; Epilepsy Genetics; Epilepsy and Neurodevelopmental Disorders; Treatment of Status Epilepticus; CTRP Channels for Antiepileptic Drugs; GABAA Receptors in Epilepsy; Milk Nutrition in Epilepsy; Ketogenic Diet for in Epilepsy…”
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Primary Mental Health Care in a New Era

Subjects: “…neurodevelopmental disorders…”
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Intelligent Soft Sensors

Subjects: “…neurodevelopmental disorders…”
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Comorbidities and Complications of Cerebral Palsy

Subjects: “…neurodevelopmental disorders…”
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The Role of Pregnancy Nutrition in Maternal and Offspring Health by Maslova, Ekaterina

Subjects: “…neurodevelopmental disorders…”
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Towards Mechanism-based Treatments for Fragile X Syndrome by Kumari, Daman

Subjects: “…neurodevelopmental disorders…”
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Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019

Subjects: “…neurodevelopmental disorder…”
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Artificial Intelligence in Medical Image Processing and Segmentation

Subjects: “…rare neurodevelopmental disorder…”
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Advances in Autism Research

Subjects: “…neurodevelopmental disorders…”
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Advances in Autism Research

Subjects: “…neurodevelopmental disorders…”
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Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies by Pachajoa H, Gomez-Pineda E, Giraldo-Ocampo S, Lores J

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Clinical Diagnosis and Management of Fetal Alcohol Spectrum Disorder and Sensory Processing Disorder in Children by Lorel Breuer, Jacob R. Greenmyer, Ted Wilson

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Common developmental trajectories and clinical identification of children with fetal alcohol spectrum disorders: A synthesis of the literature by Douglas Waite, Larry Burd

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Diagnostic path of a genetic disease: a case of Williams-Beuren syndrome in Burkina Faso by Makoura Barro, Bintou Sanogo, Aimée S. Kissou, Ad Bafa Ibrahim Ouattara, Boubacar Nacro

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How Families Manage the Complex Medical Needs of Their Children with <i>MECP2</i> Duplication Syndrome by Dani John Cherian, Daniel Ta, Jeremy Smith, Jenny Downs, Helen Leonard

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Pituitary adenylate cyclase-activating polypeptide deficient mice show length abnormalities of the axon initial segment by Misaki Iwahashi, Takeshi Yoshimura, Wakana Harigai, Kazuhiro Takuma, Hitoshi Hashimoto, Taiichi Katayama, Atsuko Hayata-Takano

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Development of an International Database for a Rare Genetic Disorder: The <i>MECP2</i> Duplication Database (MDBase) by Daniel Ta, Jenny Downs, Gareth Baynam, Andrew Wilson, Peter Richmond, Aron Schmidt, Amelia Decker, Helen Leonard

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Nabais Sa-de Vries Syndrome and Thalassemia: An Undiscovered Concurrence of SPOP and HBB Genetic Mutation by Muhammad Matloob Alam, Abdulrhman Alathaibi, Badriah Gharamah Alasmari, Mohammad Aljabri, Muhammad Kashif, Riffat Matloob, Mustafa Mohamed Selim

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Region and Cell Type Distribution of TCF4 in the Postnatal Mouse Brain by Hyojin Kim, Hyojin Kim, Noah C. Berens, Nicole E. Ochandarena, Benjamin D. Philpot, Benjamin D. Philpot, Benjamin D. Philpot

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