Search Results - "Maski, Kiran P."

Stability of nocturnal wake and sleep stages defines central nervous system disorders of hypersomnolence by Maski, Kiran P, Colclasure, Alicia, Little, Elaina, Steinhart, Erin, Scammell, Thomas E, Navidi, William, Diniz Behn, Cecilia

“…Abstract Study Objectives We determine if young people with narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia (IH) have distinct…”
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Sleep-Dependent Memory Consolidation in Children by Maski, Kiran P., MD

“…In the past 30 years, much research has been conducted elucidating the role of sleep in memory and learning; however, the interaction between sleep and…”
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Functional Neurological Symptom Disorders in a Pediatric Emergency Room: Diagnostic Accuracy, Features, and Outcome by de Gusmão, Claudio M., MD, Guerriero, Réjean M., DO, Bernson-Leung, Miya Elizabeth, MD, Pier, Danielle, MD, Ibeziako, Patricia I., MD, Bujoreanu, Simona, PhD, Maski, Kiran P., MD, Urion, David K., MD, Waugh, Jeff L., MD, PhD

“…Abstract Background In children, functional neurological symptom disorders are frequently the basis for presentation for emergency care. Pediatric…”
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Increased Pediatric Functional Neurological Symptom Disorders After the Boston Marathon Bombings: A Case Series by Guerriero, Réjean M., DO, Pier, Danielle B., MD, de Gusmão, Claudio M., MD, Bernson-Leung, Miya E., MD, Maski, Kiran P., MD, Urion, David K., MD, Waugh, Jeff L., MD, PhD

“…Abstract Background Functional neurological symptom disorders are frequently the basis for acute neurological consultation. In children, they are often…”
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Development and Implementation of a Quality Improvement Curriculum for Child Neurology Residents: Lessons Learned by Maski, Kiran P., MD, Loddenkemper, Tobias, MD, An, Sookee, BA, Allred, Elizabeth N., PhD, Urion, David K., MD, Leviton, Alan, MD

“…Abstract Background Quality improvement is a major component of the Accreditation Council for Graduate Medical Education core competencies required of all…”
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Intracranial Artery Dissection in an Adolescent With Marfan Syndrome by Maski, Kiran P., MD, Sengupta, Soma, MD, Silvera, Michelle, MD, Rivkin, Michael J., MD

“…Abstract Marfan syndrome is an autosomal dominant connective tissue disorder commonly due to mutation of the fibrillin-1 ( FBN-1 ) gene that causes disruption…”
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Sleep deprivation and neurobehavioral functioning in children by Maski, Kiran P., Kothare, Sanjeev V.

“…Sleep deprivation can result in significant impairments in daytime neurobehavioral functioning in children. Neural substrates impacted by sleep deprivation…”
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Recommended protocols for the Multiple Sleep Latency Test and Maintenance of Wakefulness Test in children: guidance from the American Academy of Sleep Medicine by Maski, Kiran P, Amos, Louella B, Carter, John C, Koch, Ellen E, Kazmi, Uzma, Rosen, Carol L

“…The American Academy of Sleep Medicine commissioned a task force of clinical experts in pediatric sleep medicine to review published literature on performing…”
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New Onset Epilepsy in Prader-Willi Syndrome: Semiology and Literature Review by Benson, Leslie A., MD, Maski, Kiran P., MD, Kothare, Sanjeev V., MD, Bourgeois, Blaise F., MD

“…Prader-Willi syndrome is a chromosomal disorder caused by absence of expression of the paternal active genes in the 15q11∼q13 chromosome region; it is…”
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Common neurological co-morbidities in autism spectrum disorders by Maski, Kiran P, Jeste, Shafali S, Spence, Sarah J

“…Autism spectrum disorders (ASDs) are heterogeneous neurodevelopmental disorders associated with various co-morbidities. Neurological co-morbidities include…”
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Quality measures for the care of patients with narcolepsy by Krahn, Lois E, Hershner, Shelley, Loeding, Lauren D, Maski, Kiran P, Rifkin, Daniel I, Selim, Bernardo, Watson, Nathaniel F

“…The American Academy of Sleep Medicine (AASM) commissioned a Workgroup to develop quality measures for the care of patients with narcolepsy. Following a…”
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Clinical Reasoning: A 14-year-boy with spells of somnolence and cognitive changes by de Gusmao, Claudio M, Maski, Kiran P, Urion, David K

“…A 14-year-old boy presented for admission after repeated episodes of lethargy and cognitive changes. He had a history of childhood absence epilepsy that had…”
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Epilepsy in Prader–Willi syndrome: Clinical characteristics and correlation to genotype by Vendrame, Martina, Maski, Kiran P, Chatterjee, Madhumouli, Heshmati, Arezou, Krishnamoorthy, Kalpathy, Tan, Wen-Hann, Kothare, Sanjeev V

“…Abstract Prader–Willi syndrome (PWS) is a genomic imprinting disease secondary to the loss of a functional paternal copy of 15q11–q13. Unlike its related…”
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Sleep deprivation and neurobehavioral functioning in children: Psychophysiology and Cognitive Neuroscience of Sleep and Sleep Disorders by MASKI, Kiran P, KOTHARE, Sanjeev V

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