Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Daphne M Hasbani"'
Publikováno v:
SSRN Electronic Journal.
Polysomnography (PSG) utilizes abbreviated electroencephalogram (EEG) to stage sleep. The aim of this study was to determine whether epileptiform abnormalities on this limited EEG coverage correlated with abnormalities on routine EEG (rEEG) and an in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3322212d3c1359aa7a506e508af4fe0c
https://doi.org/10.2139/ssrn.4096921
https://doi.org/10.2139/ssrn.4096921
Publikováno v:
Child Neurology Open, Vol 8 (2021)
Child Neurology Open
Child Neurology Open
Neurologic complications secondary to heroin abuse in the adult population have been widely described in the literature. With the recent opioid epidemic and increasing rates of heroin abuse in adolescents, pediatricians are now encountering the diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55365beb216b75f1ca7503eddf5ab73e
https://doaj.org/article/053204f10272450ab8db9fbf9dcb55b3
https://doaj.org/article/053204f10272450ab8db9fbf9dcb55b3
Autor:
Daphne M Hasbani, Aparna Polavarapu
Publikováno v:
Seminars in Pediatric Neurology. 24:70-80
Vitamins and minerals have essential functions in the body, from signal transduction to acting as cofactors for numerous enzymatic processes. Nutritional deficiencies and excess of certain vitamins and minerals can have profound effects on the centra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::432e2a4ab3da5718c2d68f6f8472783c
https://doi.org/10.1016/j.spen.2016.12.002
https://doi.org/10.1016/j.spen.2016.12.002
Publikováno v:
Clinical Case Reports
Key Clinical Message Tetrasomy X is a rare chromosomal anomaly in which sleep disorders have not been previously reported. We report on one patient with tetrasomy X and hypersomnia successfully treated with psychostimulant therapy. Sleep disorders ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7812e59d3886c363a2d1cc54b22c5ef
https://doi.org/10.1002/ccr3.1440
https://doi.org/10.1002/ccr3.1440
Autor:
Agustin Legido, Daphne M Hasbani, Darshan Lal, Ignacio Valencia, Sara McGuire, Divya S. Khurana, Gustavo Silva, Karen S. Carvalho, Joseph J. Melvin
Publikováno v:
Journal of child neurology. 35(2)
Brivaracetam is a new antiepileptic drug with limited data in children. The objective of this study was to assess the efficacy/tolerability of brivaracetam. This is a retrospective chart review of children/adolescents with refractory epilepsy treated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::924d3f5afc640d3b2d75f1906e223211
https://pubmed.ncbi.nlm.nih.gov/31617449
https://pubmed.ncbi.nlm.nih.gov/31617449
Publikováno v:
The Application of Clinical Genetics
Tuberous sclerosis complex (TSC) is a multisystem disorder that results from heterozygous mutations in either TSC1 or TSC2. The primary organ systems that are affected include the brain, skin, lung, kidney, and heart, all with variable frequency, pen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::627328cffe681713f98b0c507adac99b
http://europepmc.org/articles/PMC5189696
http://europepmc.org/articles/PMC5189696
Autor:
Daphne M, Hasbani, Peter B, Crino
Publikováno v:
Handbook of clinical neurology. 148
Tuberous sclerosis complex (TSC) is an autosomal-dominant or sporadic multisystem disorder that results from mutations in either TSC1 or TSC2. The primary organs affected include the brain, skin, lung, kidney, and heart, all with variable frequency,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c297d2d083c58df1196c87ad5ac2f44
https://pubmed.ncbi.nlm.nih.gov/29478616
https://pubmed.ncbi.nlm.nih.gov/29478616
Autor:
Daphne M Hasbani, Peter B. Crino
Tuberous sclerosis complex (TSC) is an autosomal-dominant or sporadic multisystem disorder that results from mutations in either TSC1 or TSC2. The primary organs affected include the brain, skin, lung, kidney, and heart, all with variable frequency,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deb428f3c557a5b917c8415ccee322b3
https://doi.org/10.1016/b978-0-444-64076-5.00052-1
https://doi.org/10.1016/b978-0-444-64076-5.00052-1
Autor:
Michael C. Schneider, Daphne M Hasbani, Jacqueline A. Romero, Divya S. Khurana, Imane Abdelmoumen
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 21, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports, Vol 21, Iss, Pp-(2019)
We describe a case of 5,10-methenyltetrahydrofolate synthetase (MTHFS) deficiency characterized by microcephaly, global developmental delay, epilepsy, and cerebral hypomyelination. Whole exome sequencing (WES) demonstrated homozygosity for the R74X m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ac5e81f4a764f49463a146664afbb43
https://doi.org/10.1016/j.ymgmr.2019.100545
https://doi.org/10.1016/j.ymgmr.2019.100545
Autor:
Karen S, Carvalho, Daphne M, Hasbani
Publikováno v:
Seminars in Pediatric Neurology. 25:1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc8fd53dd01f2786dfa6f0847de7447c
https://doi.org/10.1016/j.spen.2018.02.006
https://doi.org/10.1016/j.spen.2018.02.006