Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Minal V. Kekatpure"'
Autor:
Minal V Kekatpure, Venkatraman Bhat
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 1, Pp 126-129 (2020)
Externí odkaz:
https://doaj.org/article/8ec331bbdab843bdaf01c2c1dbd6c54e
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 1, Pp 131-132 (2022)
Externí odkaz:
https://doaj.org/article/b57da79762e448a6acc993e63582792e
Autor:
Minal V. Kekatpure, Sheela Nampoothiri, Kollencheri Puthenveettil Vinayan, Gopal S Pillai, A. Anand Kumar
Publikováno v:
International Journal of Epilepsy. :095-097
Symptomatic myoclonus is the major presenting feature of a small but very important and genetically diverse group of rare disorders included under the umbrella of progressive myoclonus epilepsy (PME) and progressive myoclonus ataxia (PMA) syndromes.
Autor:
Nurunisa Akyuz, Barry E. Kosofsky, Nikos Makris, Minal V. Kekatpure, Jie Liu, David N. Kennedy, Stephen J. Sheinkopf, Barry M. Lester, Brian T. Quinn, Meenakshi D. Lala
Publikováno v:
Developmental Neuroscience. 36:316-328
The brain morphometry of 21 children, who were followed from birth and underwent structural brain magnetic resonance imaging at 8-10 years, was studied. This cohort included 11 children with prenatal cocaine exposure (CE) and 10 noncocaine-exposed ch
Publikováno v:
Seminars in Cell & Developmental Biology. 20:441-454
Recent advances in MR-based brain imaging methods have provided unprecedented capabilities to visualize the brain. Application of these methods has allowed identification of brain structures and patterns of functional activation altered in offspring
Autor:
Ronald G. Crystal, Bruce M. Greenwald, Nurunisa Neyzi, Stefan Worgall, Minal V. Kekatpure, Paul J. Christos, Michael G. Kaplitt, Douglas Ballon, Madhu Mazumdar, Linda Heier, Jonathan P. Dyke, Neil R. Hackett, Barry E. Kosofsky, Dolan Sondhi, Mark M. Souweidane
Publikováno v:
Human Gene Therapy. 19:463-474
Late infantile neuronal ceroid lipofuscinosis (LINCL) is an autosomal recessive, neurodegenerative lysosomal storage disease affecting the CNS and is fatal by age 8 to 12 years. A total average dose of 2.5 10(12) particle units of an adeno-associated
Autor:
Minal V. Kekatpure, Stefan Worgall, Jonathan P. Dyke, Dikoma C. Shungu, Ronald G. Crystal, Michael G. Kaplitt, Charleen Hollmann, Barry E. Kosofsky, Mark M. Souweidane, Xiangling Mao, Dolan Sondhi, Douglas Ballon, Linda Heier, Neil R. Hackett
Publikováno v:
Neurology. 69:521-535
Background: Late infantile neuronal ceroid lipofuscinosis (LINCL) is associated with progressive degeneration of the brain and retina starting in early childhood. Methods: Thirty-two individual neurologic, ophthalmologic, and CNS imaging (MRI and MRS
Publikováno v:
Handbook of clinical neurology. 111
Neurodevelopmental disorders result from an inordinate number of genetic and environmental causes during the embryological and fetal periods of life. In the clinical setting, deciphering precise etiological diagnoses is often difficult. Newer screeni
Autor:
Nurunisa Neyzi, Jimmy T. Efird, Minal V. Kekatpure, Kalpana J. Kallianpur, Luis Gracia, James Davis, Barry E. Kosofsky, Barry M. Lester, Chris Derauf
Publikováno v:
Developmental neuroscience. 34(4)
Objective: To examine the independent contributions of prenatal methamphetamine exposure (PME) and prenatal tobacco exposure (PTE) on brain morphology among a sample of nonalcohol-exposed 3- to 5-year-old children followed prospectively since birth.
Autor:
Stefan Worgall, Dolan Sondhi, Neil R. Hackett, Barry Kosofsky, Minal V. Kekatpure, Nurunisa Neyzi, Jonathan P. Dyke, Douglas Ballon, Linda Heier, Bruce M. Greenwald, Paul Christos, Madhu Mazumdar, Mark M. Souweidane, Michael G. Kaplitt, Ronald G. Crystal
Publikováno v:
Human Gene Therapy; May2008, Vol. 19 Issue 5, p463-474, 12p