[PDF] Top 20 Natural History and Treatment of Brown’s Syndrome: Long Term Experience
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Natural History and Treatment of Brown’s Syndrome: Long Term Experience
... In conclusion, our experience seems to confirm that the spontaneous improve- ment of BS is common. This fact should be considered when evaluating BS. Furthermore, when surgery is required, planning may be complex, ... See full document
9
Safety and efficacy of long-term esomeprazole 20 mg in Japanese patients with a history of peptic ulcer receiving daily non-steroidal anti-inflammatory drugs
... of treatment with esomeprazole (20 mg once daily) in Japanese patients (aged ≥ 20 years) with endoscopic evidence of previous peptic ulcer and receiving daily oral NSAID therapy (at a stable dose) for a chronic ... See full document
9
Natural history and management of primary biliary cirrhosis
... predicting long-term outcome in PBC, more randomized clinical trials of combination fibrate and UDCA therapy with sufficient numbers and follow-up to demonstrate changes in clinical outcome should be ... See full document
11
Natural history of mevalonate kinase deficiency: a literature review
... D syndrome (HIDS), a less severe phenotype and more common form, and mevalonic aciduria (MVA), a more severe phenotype and rare ...rare long-term complications such as type AA amyloidosis, joint ... See full document
10
The natural history of interferon-α induced thyroiditis in chronic hepatitis c patients: a long term study
... established treatment available for this condi- tion is the combination ribavirin and pegylated interferon-a ...this treatment is the development of thyroid disease during ...undertaking treatment is ... See full document
5
Observations of the natural history and long term outcomes of deep venous thrombosis
... complications which usually result fi'om inaccurate placement, occlusion at the venous insertion site, throbmosis o f the inferior vena cave, new ipsilateral DVT and occasionally tears in the inferior vena cave (Blebea ... See full document
129
Obstructive sleep apnea syndrome: natural history, diagnosis, and emerging treatment options
... of treatment of OSA on cardiovascular disease, metabolic disorders, cognitive function, and road traffic accidents has already been discussed earlier in this ... See full document
23
Treatment patterns of chronic obstructive pulmonary disease in employed adults in the United States
... reliever), long-acting maintenance pharmacotherapy in patients with an exacerbation history, and short-term treatment of acute exacerbations of COPD were evalu- ated in the overall population, ... See full document
8
Neuromyelitis optica and neuromyelitis optica spectrum disorder: Natural history and long-term outcome, an Indian experience.
... There were 26 patients (female: male, 21:5), the mean age of onset of symptom was 27 years (range 9–58 years, standard deviation [SD] =12) [Figure 1]. Twenty-one patients (80%) fulfilled NMSS criteria for NMO while rest ... See full document
5
The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives
... The Brown-Vialetto-Van Laere syndrome is a rare neurological disorder which may present at all ages with sensorineural deafness, bulbar palsy and respiratory ...Fazio-Londe syndrome is considered to ... See full document
7
Natural History of Wolf-Hirschhorn Syndrome: Experience With 15 Cases
... ceptable treatment. The child was admitted to the hospital within 1 hour and 40 minutes of arrival. A previous admission for similar symptoms 10 months before this ED visit resulted in a 3-hour, 20-minute ED ... See full document
9
URTICA DIOICA (STINGING NETTLE): A REVIEW OF ITS CHEMICAL, PHARMACOLOGICAL, TOXICOLOGICAL AND ETHNOMEDICAL PROPERTIES
... catalase activity .[40,45] Also, it was found that treatment with U. dioica decreased the lipid hydroperoxide activity, indicating that the antioxidant effect of U. dioica had prevented the emergence of an oxidant ... See full document
8
West Syndrome and Lennox-Gastaut Syndrome: A Survey of Natural History
... taut syndrome are characterized by their onset in infancy and early childhood, intractable seizures occurring almost daily, severe psychomotor retardation, and poor prog-.. nosis.[r] ... See full document
10
Long term survival in pseudo Meigs’ syndrome caused by ovarian metastases from colon cancer
... A 47-year-old woman presented to the hospital with a 1-month history of abdominal distention. Physical examination revealed a huge mass in the lower abdo- men. The peripheral blood test showed elevated levels of ... See full document
5
LEARNERS' INTERACTION WITH NATURE: SOME EDUCATIONAL ISSUES
... pupils’ natural science literacy comes originally from primary school where the junior pupils study considerably a long time which is a four year period and or even ...propaedeutic natural science ... See full document
5
Long-term experience in the treatment of α1-antitrypsin deficiency: 25 years of augmentation therapy
... efficacy end-points (spirometry, diffusing capacity of the lung for carbon monoxide and shuttle walk test). Controversy remains regarding how patients with severe AATD and an initial FEV 1 >65% predicted should be ... See full document
6
PROPRANOLOL PALLIATION OF TETRALOGY OF FALLOT: EXPERIENCE WITH LONG-TERM DRUG TREATMENT IN PEDIATRIC PATIENTS
... Nonfasting serum propranolol levels in 15 pediatric patients with tetralogy of Fallot following an oral dose of propranolol ( 1 mg/kg). In eight infants blood samples were obtained two a[r] ... See full document
11
Energy crisis : prevalence, severity, treatment and persistence of fatigue after mild traumatic brain injury : a dissertation presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Psychology at Massey University, Palmerston North, New Zealand
... Successful exercise-based programmes for treatment of fatigue in illnesses such as MS and CFS were 8-12 weeks long (Fulcher & White, 1997; van Kessel et al., 2008). Programme length was set at 12 weeks ... See full document
347
A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment
... Endocrinologic pathologies in the presented patient were as follows: GH deficiency, hypothyroidism and impaired endocrine function of the pancreas. At the beginning of rGH treatment the prognosis concerning the ... See full document
9
Natural history of Sanfilippo syndrome in Spain
... Sanfilippo syndrome, is caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of heparan ...the natural history of Sanfilippo patients (MPSIIIA, MPSIIIB and ... See full document
11
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