Zobrazeno 1 - 10
of 444
pro vyhledávání: '"narp"'
Publikováno v:
Nuevo Derecho, Vol 20, Iss 35 (2024)
El presente artículo tiene como objetivo exponer un análisis sobre las barreras directas e indirectas de acceso a la justicia para la población afrodescendiente en la ciudad de Medellín. Para ello, se empleó una metodología mixta de rastreo con
Externí odkaz:
https://doaj.org/article/613935e9c76c49968ccdfc04463ad33b
Autor:
Yasunari Yamaguchi, Kazuya Okamura, Kazuhiko Yamamuro, Kazuki Okumura, Takashi Komori, Michihiro Toritsuka, Ryohei Takada, Yosuke Nishihata, Daisuke Ikawa, Takahira Yamauchi, Manabu Makinodan, Hiroki Yoshino, Yasuhiko Saito, Hideo Matsuzaki, Toshifumi Kishimoto, Sohei Kimoto
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
BackgroundSocial isolation during critical periods of development is associated with alterations in behavior and neuronal circuitry. This study aimed to investigate the immediate and developmental effects of social isolation on firing properties, neu
Externí odkaz:
https://doaj.org/article/2399da121464402f9f2969039e6207fe
Autor:
A. S. Kotov, K. V. Firsov
Publikováno v:
Русский журнал детской неврологии, Vol 17, Iss 4, Pp 63-70 (2023)
Mitochondrial dysfunction mainly affects organs with high metabolic demand, primarily the brain. Epilepsy is a common phenotypic sign of both syndromic and non-syndromic mitochondrial diseases. Epilepsy in mitochondrial diseases is poorly treatable a
Externí odkaz:
https://doaj.org/article/a3e68cc9994a4fb88666c4940ec1cf71
Publikováno v:
Jurídicas, Vol 20, Iss 2 (2023)
Una pregunta insoslayable guía el contenido de este artículo: ¿por qué la población negra, afrocolombiana, raizal y palenquera (NARP) presenta los índices de desarrollo social y económico más bajos en Colombia? La respuesta a este importante
Externí odkaz:
https://doaj.org/article/5fb1ade62d8a40138ee56e3cb740a2b6
Autor:
Piervito Lopriore, Valentina Ricciarini, Gabriele Siciliano, Michelangelo Mancuso, Vincenzo Montano
Publikováno v:
Neurology International, Vol 14, Iss 2, Pp 337-356 (2022)
Ataxia is increasingly being recognized as a cardinal manifestation in primary mitochondrial diseases (PMDs) in both paediatric and adult patients. It can be caused by disruption of cerebellar nuclei or fibres, its connection with the brainstem, or s
Externí odkaz:
https://doaj.org/article/e7fa3f7d3a72483690177dc19a93bbe4
Publikováno v:
BMC Psychiatry, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Preclinical studies have indicated that the ketamine metabolite (2R,6R)-hydroxynorketamine (HNK) is a rapid-acting antidepressant drug with limited dissociation properties and low abuse potential. However, its effects and molecula
Externí odkaz:
https://doaj.org/article/89c7e267a32c461c847d7c5cbaef1d8d
Akademický článek
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Autor:
Levenson, Eugenia
Publikováno v:
Fortune. 4/16/2007, Vol. 155 Issue 7, p51-51. 3/5p. 4 Color Photographs.
Autor:
Huijun Yuan, Keith A. Webster, Muhammad Tariq Bhatti, William W. Hauswirth, Alfred S. Lewin, John Guy
Publikováno v:
Clinical and Translational Discovery, Vol 2, Iss 3, Pp n/a-n/a (2022)
Abstract Background Mutation of the m. 8993 T > G ATP6 subunit of ATP synthase causes a maternally inherited Leigh Syndrome (LS), a rapidly fatal encephalomyelopathy in childhood called and related Neuropathy, Ataxia and Retinitis Pigmentosa (NARP) i
Externí odkaz:
https://doaj.org/article/6ccb0d57256b4c32af337b310ee758c0
Autor:
Laura Licchetta, Lorenzo Ferri, Chiara La Morgia, Corrado Zenesini, Leonardo Caporali, Maria Lucia Valentino, Raffaella Minardi, Daniela Fulitano, Lidia Di Vito, Barbara Mostacci, Lara Alvisi, Patrizia Avoni, Rocco Liguori, Paolo Tinuper, Francesca Bisulli, Valerio Carelli
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 3, Pp 704-710 (2021)
Abstract The study aims to characterize the epilepsy phenotype of maternally inherited Leigh's syndrome (MILS) and neuropathy, ataxia, retinitis pigmentosa (NARP) due to mutations in the mitochondrial ATP6 gene and to correlate electroclinical featur
Externí odkaz:
https://doaj.org/article/e690895416d44998b922be907eb744e1