B Acar-Perk, J Weimer, K Koch, A Salmassi… - Human …, 2011 - ESHRE Page 1. i278 Abstracts of the 27th Annual Meeting of ESHRE, Stockholm, Sweden, 3 July – 6 July, 2011 Results: 10648 AID cycles were performed from January,2007 to September, 2009 in our Hospital and resulted in 2364 ...
LP Zebala, KH Bridwell, C Baldus… - Journal of Pediatric …, 2011 - journals.lww.com ... Level of Evidence: Case Series; Level IV. Spinalmuscularatrophy (SMA) is a progressive flaccid neuromuscular disorder affecting anterior horn cells with a wide spectrum of clinical manifestations. 1–5 Disorder severity is related ... Related articles - All 3 versions
VM Richon, PA Marks… - US Patent App. 13/017,447, 2011 - Google Patents ... 0047] 3. Other forms of familial spinalmuscular atro- phy [0048] C. Primary lateral sclerosis [0049] D. Hereditary spastic paraplegia [0050] VII. Syndromes combining muscular weakness and wasting with sensory changes (progressive neural muscu- lar atrophy; chronic familial ... All 2 versions
[PDF] from peerproject.euJ Raaphorst, M de Visser, MJ van Tol… - Journal of Neurology, …, 2011 - jnnp.bmj.com ... Abstract. Aim In contrast with findings in amyotrophic lateral sclerosis (ALS), cognitive impairments have as yet not been shown in the lower motor neuron variant of motor neuron disease, progressivespinalmuscularatrophy (PMA). ... Related articles - All 6 versions
[HTML] from rupress.orgA Sen, T Yokokura, MW Kankel… - The Journal of Cell …, 2011 - jcb.rupress.org ... Introduction. Spinalmuscularatrophy (SMA) is an inherited neurodegenerative disease causing progressive deterioration of motor functions and loss of motor neurons (Azzouz et al., 2004). After cystic fibrosis, SMA is the most ... Cited by 1 - Related articles - All 2 versions
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