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Multi-system neurological disorder associated with a CRYAB variant.
Sadeh M, Rahat D, Meiner V, Fellig Y, Arad M, Schueler-Furman O, Hu Y, Li Y, Bönnemann CG, Lossos A. Sadeh M, et al. Neurogenetics. 2021 May;22(2):117-125. doi: 10.1007/s10048-021-00640-x. Epub 2021 Apr 3. Neurogenetics. 2021. PMID: 33811585
Early clinical heterogeneity in choreoacanthocytosis.
Lossos A, Dobson-Stone C, Monaco AP, Soffer D, Rahamim E, Newman JP, Mohiddin S, Fananapazir L, Lerer I, Linetsky E, Reches A, Argov Z, Abramsky O, Gadoth N, Sadeh M, Gomori JM, Boher M, Meiner V. Lossos A, et al. Among authors: sadeh m. Arch Neurol. 2005 Apr;62(4):611-4. doi: 10.1001/archneur.62.4.611. Arch Neurol. 2005. PMID: 15824261
Frequent misdiagnosis of adult polyglucosan body disease.
Hellmann MA, Kakhlon O, Landau EH, Sadeh M, Giladi N, Schlesinger I, Kidron D, Abramsky O, Reches A, Argov Z, Rabey JM, Chapman J, Rosenmann H, Gal A, Moshe Gomori J, Meiner V, Lossos A. Hellmann MA, et al. Among authors: sadeh m. J Neurol. 2015 Oct;262(10):2346-51. doi: 10.1007/s00415-015-7859-4. Epub 2015 Jul 21. J Neurol. 2015. PMID: 26194201
Glycogen Debrancher Enzyme Deficiency Myopathy.
Sadeh M, Yosovich K, Dabby R. Sadeh M, et al. J Clin Neuromuscul Dis. 2021 Jun 1;22(4):224-227. doi: 10.1097/CND.0000000000000339. J Clin Neuromuscul Dis. 2021. PMID: 34019008
253 results