Publications by authors named "T Kimball"

Essential hypertension is one of the most common conditions managed in pediatric cardiology and can result in lasting deleterious effects on the cardiovascular system. Pediatric hypertension is so prevalent in the United States that it is often referred to as a public health challenge. Social determinants of health (SDH) are the cultural, economic, educational, healthcare accessibility, and political influences in the environment in which an individual is born or lives, all of which can affect that individual's overall health.

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Spontaneous intracerebral hemorrhage(ICH) represents a life-threatening form of stroke, marked by its impact on survival and quality of life. ICH can be categorized from monogenic disorders linked to causal germline variants in ICH-related genes to complex sporadic cases, highlighting the interaction among lifestyle factors, environmental influences, and genetic components in determining risk. Among sporadic ICH, the influence of these factors varies across ICH subtypes, evidenced by heritability rates of up to 73% for lobar ICH versus 34% for non-lobar ICH.

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Ischemic stroke is a major cause of mortality and disability and has become a significant public health concern among women. Overall, women have more ischemic stroke events than men, in part due to their longer life span, and also suffer from more severe stroke-related disabilities compared to men. Women are also more likely than men to present with atypical non-focal neurological symptoms, potentially leading to delayed diagnosis and treatment.

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Article Synopsis
  • Fabry disease (FD) is a rare genetic disorder caused by mutations in the GLA gene, resulting in various symptoms, and this study analyzed the characteristics of 52 Mexican FD patients.* -
  • Common symptoms included acroparesthesias, hypohidrosis, heat intolerance, and proteinuria, with more severe renal and neurological issues observed in males; additional findings included cardiac problems and specific skin manifestations.* -
  • The study identified a novel genetic variant associated with an atypical FD phenotype that could resemble Multiple Sclerosis, highlighting the need for renal biopsies for accurate diagnosis when FD is suspected.*
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