Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Gayatra Mainali"'
Autor:
Zahra Zhu, Daniela Dluzynski, Nouran Hammad, Deepika Pugalenthi, Sarah A. Walser, Rea Mittal, Debopam Samanta, Melanie L. Brown, Ali A. Asadi-Pooya, Angelina Kakooza-Mwesige, Alberto Spalice, Martina Capponi, Alain Lekoubou, Ashutosh Kumar, Sita Paudel, Paul R. Carney, Gayatra Mainali, Sunil Naik
Publikováno v:
Children, Vol 10, Iss 4, p 713 (2023)
(1) Background: Epilepsy is one of the most common chronic neurological disorders in childhood. Complementary and alternative medicine (CAM) use is highly prevalent in patients with epilepsy. Despite CAM’s widespread and increasing popularity, its
Externí odkaz:
https://doaj.org/article/42908ae6704f43b8a55c00b647b16976
Publikováno v:
Case Reports in Genetics, Vol 2022 (2022)
Autosomal recessive intellectual developmental disorder type 5 (MRT5, OMIM # 611091) is caused by biallelic pathogenic variants, leading to loss of function of the NSUN2 gene which encodes a methyltransferase involved in several biological processes,
Externí odkaz:
https://doaj.org/article/be0a10a830274554a593f75e9a99a547
Autor:
Kyra Newmaster, Zahra Zhu, Elizabeth Bolt, Ryan J. Chang, Christopher Day, Asmaa Mhanna, Sita Paudel, Osman Farooq, Arun Swaminathan, Prakrati Acharya, Wisit Cheungpasitporn, Siddharth Gupta, Debopam Samanta, Naeem Mahfooz, Gayatra Mainali, Paul R. Carney, Sunil Naik
Publikováno v:
Children, Vol 9, Iss 9, p 1372 (2022)
Ketogenic diets (KDs) are highly effective in the treatment of epilepsy. However, numerous complications have been reported. During the initiation phase of the diet, common side effects include vomiting, hypoglycemia, metabolic acidosis and refusal o
Externí odkaz:
https://doaj.org/article/ed72503ac37c4abbb584d1fa12aa323d
Autor:
Zahra Zhu, Rea Mittal, Sarah A. Walser, Erik Lehman, Ashutosh Kumar, Sita Paudel, Gayatra Mainali
Publikováno v:
Journal of Child Neurology. 37:334-339
Complementary and alternative medicine (CAM) use by the pediatric population with epilepsy in rural Pennsylvania was studied to characterize the prevalence, perceived effectiveness, and reasons for CAM use. This study additionally assessed the adequa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bc86f8d2200ca0afa444507ae4d5cd2
https://doi.org/10.1177/08830738211069790
https://doi.org/10.1177/08830738211069790
Publikováno v:
American Journal of Case Reports. 23
BACKGROUND The relatively new autoimmune disorder, anti-myelin oligodendrocyte glycoprotein (MOG) disease is particularly interesting because of its broad range of presentations. This entity's appearance on magnetic resonance imaging (MRI) of the bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400dbf2a0389b199c12a169b1225a3fd
https://doi.org/10.12659/ajcr.936361
https://doi.org/10.12659/ajcr.936361
Autor:
Gayatra Mainali, Erik Lehman, Himadri Patel, Laura Duda, Kieu Hanh Nguyen, Debra Byler, Ashutosh Kumar
Publikováno v:
Journal of Child Neurology. 35:512-516
Introduction: Tourette syndrome is a neuropsychiatric condition defined by motor and phonic tics with onset in childhood. Many families have concerns regarding potential side effects of pharmacologic treatments, and often have difficulty accessing co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd8c8888753069e5d807e8450223ad10
https://doi.org/10.1177/0883073820913670
https://doi.org/10.1177/0883073820913670
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3cb6893d62e257d4ffccf8b4282f6f3
https://doi.org/10.7759/cureus.22919
https://doi.org/10.7759/cureus.22919
Publikováno v:
Child Neurology Open. 10:2329048X2311710
A 17-year-old female with sickle cell disease status post a recent stem cell transplant and on tacrolimus developed an acute expressive aphasia, dysphagia, and drooling. Brain MRI revealed diffuse restricted diffusion involving the bilateral corona r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b26651a95b7d87a0e583964839b94996
https://doi.org/10.1177/2329048x231171011
https://doi.org/10.1177/2329048x231171011
Publikováno v:
Child Neurology Open, Vol 8 (2021)
Child Neurology Open
Child Neurology Open
Pitt Hopkins-like syndrome 1 (PTHLS1, OMIM # 610042) is an ultra-rare autosomal recessive condition with a prevalence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc09df1bd104e3a65fdcb99e779c278f
https://doaj.org/article/5c670dfe6da54ef7bc68e6fb0e7b9143
https://doaj.org/article/5c670dfe6da54ef7bc68e6fb0e7b9143
Publikováno v:
Child Neurology Open
Infection-induced acute encephalopathy 3 (IIAE3) is an autosomal dominant disease resulting from a pathogenic variant in the RANBP2 gene. IIAE3 results in the susceptibility to the recurrence of acute necrotizing encephalopathy (ANE1) which presents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71293cb7baba73c04ed065d9a7c80bd7
http://europepmc.org/articles/PMC8326991
http://europepmc.org/articles/PMC8326991