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Page 1
Distal Hereditary Motor Neuronopathy of the Jerash Type.
Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, El-Khateeb M, Al-Qudan A, Horany K. Middleton LT, et al. Among authors: neocleous v. Ann N Y Acad Sci. 1999 Oct;883(1):65-68. doi: 10.1111/j.1749-6632.1999.tb08569.x. Ann N Y Acad Sci. 1999. PMID: 29086969
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene.
Middleton L, Ohno K, Christodoulou K, Brengman J, Milone M, Neocleous V, Serdaroğlu P, Deymeer F, Ozdemir C, Mubaidin A, Horany K, Al-Shehab A, Mavromatis I, Mylonas I, Tsingis M, Zamba E, Pantzaris M, Kyriallis K, Engel AG. Middleton L, et al. Among authors: neocleous v. Neurology. 1999 Sep 22;53(5):1076-82. doi: 10.1212/wnl.53.5.1076. Neurology. 1999. PMID: 10496269
Distal hereditary motor neuronopathy of the Jerash type.
Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, el-Khateeb M, al-Qudah A, Horany K. Middleton LT, et al. Among authors: neocleous v. Ann N Y Acad Sci. 1999 Sep 14;883:65-8. Ann N Y Acad Sci. 1999. PMID: 10586232
Distal hereditary motor neuronopathy of the Jerash type.
Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, el-Khateeb M, al-Qudah A, Horany K. Middleton LT, et al. Among authors: neocleous v. Ann N Y Acad Sci. 1999 Sep 14;883:439-42. Ann N Y Acad Sci. 1999. PMID: 10586267 No abstract available.
High carrier frequency of 21-hydroxylase deficiency in Cyprus.
Phedonos AA, Shammas C, Skordis N, Kyriakides TC, Neocleous V, Phylactou LA. Phedonos AA, et al. Among authors: neocleous v. Clin Genet. 2013 Dec;84(6):585-8. doi: 10.1111/cge.12153. Epub 2013 Apr 22. Clin Genet. 2013. PMID: 23600966
Distal Hereditary Motor Neuronopathy of the Jerash Type.
Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, El-Khateeb M, Al-Qudah A, Horany K. Middleton LT, et al. Among authors: neocleous v. Ann N Y Acad Sci. 1999 Oct;883(1):439-442. doi: 10.1111/j.1749-6632.1999.tb08604.x. Ann N Y Acad Sci. 1999. PMID: 29086938 No abstract available.
COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy.
Voskarides K, Damianou L, Neocleous V, Zouvani I, Christodoulidou S, Hadjiconstantinou V, Ioannou K, Athanasiou Y, Patsias C, Alexopoulos E, Pierides A, Kyriacou K, Deltas C. Voskarides K, et al. Among authors: neocleous v. J Am Soc Nephrol. 2007 Nov;18(11):3004-16. doi: 10.1681/ASN.2007040444. Epub 2007 Oct 17. J Am Soc Nephrol. 2007. PMID: 17942953
Familial Mediterranean fever associated with MEFV mutations in a large cohort of Cypriot patients.
Neocleous V, Costi C, Kyriakou C, Kyriakides TC, Shammas C, Skordis N, Toumba M, Kyriakou S, Koliou M, Kousparou M, Onoufriou M, Hadjipanayis A, Iasonides M, Atamyan VN, Pierides A, Christophidou-Anastasiadou V, Tanteles GA, Phylactou LA. Neocleous V, et al. Ann Hum Genet. 2015 Jan;79(1):20-7. doi: 10.1111/ahg.12087. Epub 2014 Nov 13. Ann Hum Genet. 2015. PMID: 25393764
73 results