نتایج جستجو برای: basal ganglia calcifications

تعداد نتایج: 116877  

Journal: :Journal of Anatomy 2000

Elham Pourbakhtyaran, Mohammad Hadi Gharedaghi, Mohammad Salehi Sadaghiani, Sara Esmaeili, Yashar Yousefzadeh-fard,

Introduction: Addiction imposes a large medical, social and economic burden on societies. Currently, there is no effective treatment for addiction. Our struggle to decipher the different mechanisms involved in addiction requires a proper understanding of the brain regions which promote this devastating behavior. Previous studies have shown a pivotal role for insula in cigarette smoking. In this...

Journal: :Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion 2013
Antonia García-Martín Rebeca Reyes-García José Miguel García-Castro Manuel Muñoz-Torres

Mitochondrial DNA mutations are uncommon causes of diabetes mellitus in adults and are related to a wide spectrum of diseases. Its association with myopathy, lactic acidosis, and stroke is an even less frequent syndrome. We report the case of a young woman who was diagnosed with mitochondrial disease upon admission for a stroke. This case is that of a 46-year-old patient urgently admitted to th...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1996
G M Fabrizi E Cardaioli G S Grieco T Cavallaro A Malandrini L Manneschi M T Dotti A Federico G Guazzi

OBJECTIVE To verify the phenotype to genotype correlations of mitochondrial DNA (mtDNA) related disorders in an atypical maternally inherited encephalomyopathy. METHODS Neuroradiological, morphological, biochemical, and molecular genetic analyses were performed on the affected members of a pedigree harbouring the heteroplasmic A to G transition at nucleotide 3243 of the mitochondrial tRNALeu(...

2003
Gian Maria Fabrizi Elena Cardaioli Gaetano Salvatore Tiziana Cavallaro Alessandro Malandrini Letizia Manneschi Maria Teresa Dotti Antonio Federico Giancarlo Guazzi

Received 31 October 1995 and in final revised form 19 February 1996 Accepted 23 February 1996 Abstract Objective-To verify the phenotype to genotype correlations of mitochondrial DNA (mtDNA) related disorders in an atypical maternally inherited encephalomyopathy. Methods-Neuroradiological, morphological, biochemical, and molecular genetic analyses were performed on the affected members of a ped...

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