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1  a mechanism responsible for postspaceflight orthostatic intolerance.
2 chanism underlying individual variability in orthostatic intolerance.
3 iciency is linked to tachycardia in familial orthostatic intolerance.
4  changes that might contribute to postflight orthostatic intolerance.
5  that may contribute to, rather than offset, orthostatic intolerance.
6 ts in the treatment of patients with chronic orthostatic intolerance.
7 povolemia alone, potentially contributing to orthostatic intolerance.
8 ributes to the pathophysiologic mechanism of orthostatic intolerance.
9 underlie hyperadrenergic states that lead to orthostatic intolerance.
10 an norepinephrine transporter contributes to orthostatic intolerance.
11                Women are more susceptible to orthostatic intolerance.
12 y are likely responsible for the symptoms of orthostatic intolerance across the menstrual cycle in wo
13 are probably responsible for the symptoms of orthostatic intolerance across the menstrual cycle in wo
14                                              Orthostatic intolerance after bed rest is characterized
15                            In a patient with orthostatic intolerance and her relatives, we measured p
16                                      Chronic orthostatic intolerance associated with postural tachyca
17  Starling relationship, which contributes to orthostatic intolerance by causing an excessive reductio
18 rdiovascular adaptation to bed rest leads to orthostatic intolerance, characterized by an excessive f
19                                      Chronic orthostatic intolerance (COI) is a debilitating autonomi
20                                      Chronic orthostatic intolerance (COI) occurs in postural tachyca
21 s during head-up tilt (HUT) in patients with orthostatic intolerance during daily life, and to identi
22 orthostatic tolerance during cold stress and orthostatic intolerance during heat stress.
23  by echocardiogram, weight loss > 10 pounds, orthostatic intolerance, fatigue) in combination were hi
24                     Patients with idiopathic orthostatic intolerance had lower cardiac vagal barorefl
25                     Patients with idiopathic orthostatic intolerance have lower cardiac vagal baroref
26 ion between the chronic fatigue syndrome and orthostatic intolerance; however, treatment with the sal
27 the heart' is implicated in certain types of orthostatic intolerance in humans.
28 ation therapy are more effective in treating orthostatic intolerance in patients with CFS.
29 lt-table testing may be indicated to confirm orthostatic intolerance in subjects with UARS.
30           HUT fails to reproduce symptoms of orthostatic intolerance in the majority of patients.
31                                              Orthostatic intolerance is a syndrome characterized by l
32                                              Orthostatic intolerance is characterized by postural tac
33                                              Orthostatic intolerance is common when astronauts return
34 uced red blood cell masses, hypovolaemia and orthostatic intolerance, marked by greater cardio-accele
35  mild syndrome of orthostatic tachycardia or orthostatic intolerance may appear.
36 ia syndrome (POTS) induces disabling chronic orthostatic intolerance notable for an excessive increas
37  repeated neurocardiogenic presyncope (NCS), orthostatic intolerance occurs without persistent sympat
38 ed by tilt-table testing on 15 subjects with orthostatic intolerance (OI) and UARS, five normotensive
39                                      Chronic orthostatic intolerance (OI) is characterized by symptom
40 in an individual with the autonomic disorder orthostatic intolerance (OI).
41           Patients diagnosed with idiopathic orthostatic intolerance report symptoms of lightheadedne
42          Peak work capacity, activity level, orthostatic intolerance, salivary cortisol, and natural
43 (P< .001), primarily due to elevation of the orthostatic intolerance, secretomotor, upper gastrointes
44          Young women are more susceptible to orthostatic intolerance than men, though the sex-specifi
45 ia syndrome (POTS) induces disabling chronic orthostatic intolerance with an excessive increase in he
46 re commonly used in the treatment of chronic orthostatic intolerance with postural tachycardia syndro
47 m onset (hazard ratio 1.67, P < 0.003); (iv) orthostatic intolerance within 1 year of symptom onset (
48 e hypothesized that patients with idiopathic orthostatic intolerance would have impaired cardiac vaga

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