Pompe disease is an autosomal recessive lysosomal storage disorder characterized by progressive myopathy with proximal muscle weakness, respiratory muscle dysfunction, and cardiomyopathy. Its prevalence ranges...
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Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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! # Ola via Alexandros G.Sfakianakis on Inoreader
Η λίστα ιστολογίων μου
Δευτέρα 29 Οκτωβρίου 2018
Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report
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- Endoscopic Transcanal Autologous Cartilage Ossicul...
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- PentoxIfylline and Tocopherol for the Treatment of...
- GP-induced Chemotherapy Combined With IMRT and TPF...
- An Algorithmic Approach to the Treatment of Fronta...
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- Mitteilungen DGKFO
- 59/w mit Erosionen an Mund- und Nasenschleimhaut
- Die AG JuDerm des BVDD
- 20/w mit plötzlich auftretendem, ausgeprägtem Haar...
- 40/m mit Fluor urethralis
- 85/m mit Blasen am gesamten Integument
- 77/w mit persistierenden rötlichen und schuppenden...
- Panorama Dermatologische Praxis
- 46/w mit juckenden Hautveränderungen in den seborr...
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- 57/m mit hyperkeratotischen Knoten am rechten Unte...
- 67/w mit erythematös-schuppenden Plaques am Abdome...
- 46/m mit Pusteln an Hand- und Fußsohlen
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- Commentary on letter to editor titled “surgical ma...
- Mitteilungen DGKFO
- Defining Pollen Seasons: Background and Recommenda...
- Impact of community respiratory viral infections i...
- Expression of human and Porphyromonas gingivalis g...
- Comparative analysis of blood parameters of the er...
- Defining Pollen Seasons: Background and Recommenda...
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- Regorafenib or rechallenge chemotherapy: which is ...
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