[HTML][HTML] Symptom presentation and access to medical care in patients with postural orthostatic tachycardia syndrome: role of sex
Background Postural orthostatic tachycardia syndrome (POTS) is a chronic form of
orthostatic intolerance that primarily impacts female patients of childbearing age. The role of …
orthostatic intolerance that primarily impacts female patients of childbearing age. The role of …
Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders
M Vazquez, J Chovanec, J Kim, T DiMaggio… - Human Genetics and …, 2022 - cell.com
Hereditary alpha-tryptasemia (HαT) is an autosomal dominant (AD) genetic trait
characterized by elevated basal serum tryptase≥ 8 ng/mL, caused by increased α-tryptase …
characterized by elevated basal serum tryptase≥ 8 ng/mL, caused by increased α-tryptase …
Idiopathic osteoporosis, Ehlers–Danlos syndrome, postural orthostatic tachycardia syndrome, and mast cell activation disorder in a 27‐year‐old male patient: A …
C Rattray - Clinical Case Reports, 2022 - Wiley Online Library
A young male patient presents with widespread pain and varying chronic inflammatory
symptoms for three years and idiopathic low bone density for more than ten years. Based on …
symptoms for three years and idiopathic low bone density for more than ten years. Based on …
[HTML][HTML] Nutritional knowledge, attitudes and dietary behaviours amongst individuals with hypermobility syndromes and associations with co-morbid gastrointestinal …
N Paiba, M Harris - European Journal of Integrative Medicine, 2023 - Elsevier
Abstract Introduction Hypermobile Ehlers–Danlos syndrome (hEDS) and hypermobility
spectrum disorder (HSD) are hereditary connective tissue disorders involving joint …
spectrum disorder (HSD) are hereditary connective tissue disorders involving joint …
[PDF][PDF] MAR Pediatrics (2024) 5: 3 Research Article
AJ Maxwell, D Wardly - 2024 - researchgate.net
We describe a clinical phenotype we have characterized and have been presenting over the
past half-decade whereby the combination of a genetically vulnerable host and a chronic …
past half-decade whereby the combination of a genetically vulnerable host and a chronic …
[HTML][HTML] Anàlisi de les reaccions adaptatives del sistema nerviós autònom
AC Castro - 2023 - dialnet.unirioja.es
La conciencia corporal y la reactividad del sistema nervioso alteradas son características
que se han evidenciado en distintas enfermedades de salud mental como son los trastornos …
que se han evidenciado en distintas enfermedades de salud mental como son los trastornos …
[PDF][PDF] Maribel Vazquez, Jack Chovanec, Jiwon Kim, Thomas DiMaggio, Joshua D. Milner, 2
CA Francomano, CA Gurnett, M Ritelli, M Colombi… - scholarworks.iupui.edu
Hereditary alpha-tryptasemia (HaT) is an autosomal dominant (AD) genetic trait
characterized by elevated basal serum tryptase R8 ng/mL, caused by increased a-tryptase …
characterized by elevated basal serum tryptase R8 ng/mL, caused by increased a-tryptase …
[引用][C] Understanding the Connection Between Mast Cell Activation Syndrome and Excessive Menstrual Bleeding
M McKean