HuGE Literature Finder
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| Genotype-Phenotype Correlation of SMN1 and NAIP Deletions in Korean Patients with Spinal Muscular Atrophy. Journal of clinical neurology (Seoul, Korea) 2016 Oct . Ahn Eun Ji, Yum Mi Sun, Kim Eun Hee, Yoo Han Wook, Lee Beom Hee, Kim Gu Hwan, Ko Tae Su |
| Genetic findings of Cypriot spinal muscular atrophy patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Oct 36 (10): 1829-34. Theodorou L, Nicolaou P, Koutsou P, Georghiou A, Anastasiadou V, Tanteles G, Kyriakides T, Zamba-Papanicolaou E, Christodoulou |
| Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients. Journal of human genetics 2015 Aug . Brkušanin Miloš, Kosa? Ana, Jovanovi? Vladimir, Pešovi? Jovan, Brajuškovi? Goran, Dimitrijevi? Nikola, Todorovi? Slobodanka, Romac Stanka, Mili? Raši? Vedrana, Savi?-Pavi?evi? Dušan |
| Association of copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein gene with the natural history in a Chinese spinal muscular atrophy cohort. Journal of child neurology 2015 Mar 30 (4): 429-36. Qu Yu-jin, Ge Xiu-shan, Bai Jin-li, Wang Li-wen, Cao Yan-yan, Lu Yan-yu, Jin Yu-wei, Wang Hong, Song Fa |
| [Analysis and carrier screening for copy numbers of SMN and NAIP genes in children with spinal muscular atrophy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2014 Apr 31 (2): 152-5. Zeng Guangqun, Zheng Hong, Cheng Jing, Chen Rong, Lin He, Yang Jiyun, Zhang Dingdi |
| Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran. Advanced biomedical research 2014 3 74. Sedghi Maryam, Behnam Mahdiyeh, Fazel Esmat, Salehi Mansoor, Ganji Hamid, Meamar Rokhsareh, Hosseinzadeh Majid, Nouri Nayer |
| Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy. Brain & development 2009 Jan 31 (1): 42-5. Watihayati Mohd Shamshudin, Fatemeh Hayati, Marini Marzuki, Atif Amin Baig, Zahiruddin Wan Mohd, Sasongko Teguh Haryo, Tang Thean Hock, Zabidi-Hussin Z A M H, Nishio Hisahide, Zilfalil Bin Al |
| Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy. Journal of Zhejiang University. Science. B 2009 Jan 10 (1): 29-34. Liang Yu-hua, Chen Xiao-ling, Yu Zhong-sheng, Chen Chun-yue, Bi Sheng, Mao Lian-gen, Zhou Bo-lin, Zhang Xian-ni |
| Phenotype modifiers of spinal muscular atrophy: the number of SMN2 gene copies, deletion in the NAIP gene and probably gender influence the course of the disease. Acta biochimica Polonica 2009 56 (1): 103-8. Jedrzejowska Maria, Milewski Micha?, Zimowski Janusz, Borkowska Janina, Kostera-Pruszczyk Anna, Sielska Danuta, Jurek Marta, Hausmanowa-Petrusewicz Ire |
| Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy. Annals of the Academy of Medicine, Singapore 2007 Nov 36 (11): 937-41. Derakhshandeh-Peykar Pupak, Esmaili Mohsen, Ousati-Ashtiani Zahra, Rahmani Manijeh, Babrzadeh Farbod, Farshidi Shahla, Attaran Elham, Sajedifar Mohammad Mehdi, Farhud Dariush Daneshv |
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