Francesca R Lepri Selected Research

Epilepsy (Aura)

1/2020

Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function.

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Francesca R Lepri Research Topics

Disease

1	Sleep Initiation and Maintenance Disorders (Insomnia) 01/2020
1	Congenital Disorders of Glycosylation 01/2020
1	Inborn Genetic Diseases (Disease, Hereditary) 01/2020
1	Intellectual Disability (Idiocy) 01/2020
1	KBG syndrome 01/2020
1	Epilepsy (Aura) 01/2020
1	Cognitive Dysfunction 01/2019
1	Glycogen Storage Disease Type III (Cori's Disease) 01/2019
1	Neoplasms (Cancer) 01/2019
1	Noonan Syndrome (Female Pseudo-Turner Syndrome) 01/2019
1	Facies 01/2019

Drug/Important Bio-Agent (IBA)

1	Proteins (Proteins, Gene)FDA Link 01/2020
1	Biomarkers (Surrogate Marker)IBA 01/2020
1	LipidsIBA 01/2020
1	HDL CholesterolIBA 01/2020
1	EnzymesIBA 01/2019
1	Hormones (Hormone)IBA 01/2019
1	CytokinesIBA 01/2019
1	Intercellular Signaling Peptides and Proteins (Growth Factors)IBA 01/2019