Works matching IS 26330040 AND DT 2022 AND VI 3
Results: 16
Telehealth for patients with rare epilepsies.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221076861
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- Publication type:
- Article
Therapeutic angiogenesis in Buerger's disease: reviewing the treatment landscape.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040211070295
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- Publication type:
- Article
Racial differences in the dermatological manifestations of tuberous sclerosis complex and the potential effects on diagnosis and care.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221140125
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- Publication type:
- Article
End-stage crystalline maculopathy with retinal atrophy in Sjögren-Larsson syndrome: a case report and review of the literature.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221122496
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- Publication type:
- Article
What are the benefits of the anti-FGF23 antibody burosumab on the manifestations of X-linked hypophosphatemia in adults in comparison with conventional therapy? A review.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221074702
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- Publication type:
- Article
Quality of life in Barth syndrome.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221093743
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- Publication type:
- Article
Building cross-border collaborations to increase diversity and accelerate rare disease drug development -- meeting report from the inaugural IndoUSrare Annual Conference 2021.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221133124
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- Article
Clinical evidence of interventions assessed in Friedreich ataxia: a systematic review.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221139872
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- Publication type:
- Article
Primary ovarian malignant mixed Müllerian tumor: a rare case report.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221107389
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- Publication type:
- Article
Impact of the Covid-19 epidemic on a US sample of patients with myasthenia gravis.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221082673
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- Article
Congenital disorder of glycosylation -- one size does not fit all: a parent's perspective.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221118099
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- Article
Pharmacology update: pamidronate for hypertrophic pulmonary osteoarthropathy in palliative care.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040211070298
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- Publication type:
- Article
'Granulomatosis with polyangiitis after Pfizer vaccination': a case report.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221130084
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- Publication type:
- Article
Mannose treatment improves immune deficiency in mannose phosphate isomerase--congenital disorder of glycosylation: case report and review of literature.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040211091283
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- Publication type:
- Article
Future of genetic therapies for rare genetic diseases: what to expect for the next 15 years?
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221100840
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- Publication type:
- Article
A Systematic Review investigating the Effectiveness of Exercise training in Glycogen Storage Diseases.
- Published in:
- Therapeutic Advances in Rare Disease, 2022, v. 3, p. 1, doi. 10.1177/26330040221076497
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- Publication type:
- Article