Narlı N - Search Results

1

A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease.

Calì E, Lin SJ, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M, Mankad K, Galanaki E, Efthymiou S, Sudhakar S, Athanasiou-Fragkouli A, Çelik T, Narlı N, Bianca S, Murphy D, De Carvalho Moreira FM; SYNaPS Study Group; Andrea Accogli, Petree C, Huang K, Monastiri K, Edizadeh M, Nardello R, Ognibene M, De Marco P, Ruggieri M, Zara F, Striano P, Şahin Y, Al-Gazali L, Abi Warde MT, Gerard B, Zifarelli G, Beetz C, Fortuna S, Soler M, Valente EM, Varshney G, Maroofian R, Salpietro V, Houlden H. Calì E, et al. Among authors: narli n. Genet Med. 2022 Oct;24(10):2194-2203. doi: 10.1016/j.gim.2022.07.013. Epub 2022 Aug 24. Genet Med. 2022. PMID: 36001086 Free PMC article.

2

A neonate with homozygous protein C deficiency with a homozygous Arg178Trp mutation.

Ozlu F, Kyotani M, Taskin E, Ozcan K, Kojima T, Matsushita T, Yapicioğlu H, Takagi A, Saşmaz I, Satar M, Narli N. Ozlu F, et al. Among authors: narli n. J Pediatr Hematol Oncol. 2008 Aug;30(8):608-11. doi: 10.1097/MPH.0b013e318179a15d. J Pediatr Hematol Oncol. 2008. PMID: 18799939

3

Erythrocyte pyruvate kinase activity in term and preterm infants.

Narli N, Satar M, Atici A, Kayrin L. Narli N, et al. Pediatr Hematol Oncol. 1998 Jan-Feb;15(1):63-7. doi: 10.3109/08880019809009509. Pediatr Hematol Oncol. 1998. PMID: 9509507

4

A newborn infant with sternal malformation/vascular dysplasia association.

Yapicioğlu H, Narli N, Satar M, Soyupak S, Küçükosmanoğlu O. Yapicioğlu H, et al. Among authors: narli n. Genet Couns. 2002;13(1):35-9. Genet Couns. 2002. PMID: 12017236

5

Sonographic measurements of the liver, spleen and kidney dimensions in the healthy term and preterm newborns.

Soyupak SK, Narli N, Yapicioğlu H, Satar M, Aksungur EH. Soyupak SK, et al. Among authors: narli n. Eur J Radiol. 2002 Jul;43(1):73-8. doi: 10.1016/s0720-048x(01)00466-1. Eur J Radiol. 2002. PMID: 12065125

6

Intraventricular streptokinase for the treatment of posthaemorrhagic hydrocephalus of preterm.

Yapicioğlu H, Narli N, Satar M, Soyupak S, Altunbaşak S. Yapicioğlu H, et al. Among authors: narli n. J Clin Neurosci. 2003 May;10(3):297-9. doi: 10.1016/s0967-5868(03)00028-6. J Clin Neurosci. 2003. PMID: 12763331

7

Schwartz-Jampel syndrome: three pediatric case reports.

Yapicioğlu H, Satar M, Yildizdaş D, Narli N, Suleymanova D, Tutak E. Yapicioğlu H, et al. Among authors: narli n. Genet Couns. 2003;14(3):353-8. Genet Couns. 2003. PMID: 14577682

8

Serum insulin-like growth factor 1 and growth hormone levels of hypoxic-ischemic newborns.

Satar M, Ozcan K, Yapicioğlu H, Narli N. Satar M, et al. Among authors: narli n. Biol Neonate. 2004;85(1):15-20. doi: 10.1159/000074952. Epub 2003 Nov 19. Biol Neonate. 2004. PMID: 14631161

9

A newborn infant with generalized glutathione synthetase deficiency.

Yapicioğlu H, Satar M, Tutak E, Narli N, Topaloğlu AK. Yapicioğlu H, et al. Among authors: narli n. Turk J Pediatr. 2004 Jan-Mar;46(1):72-5. Turk J Pediatr. 2004. PMID: 15074378

10

Is oral indomethacin effective in treatment of preterm infants with patent ductus arteriosus?

Satar M, Yapicioğlu H, Narli N, Ozbarlas N, Küçükosmanoğlu O, Tutak E. Satar M, et al. Among authors: narli n. Turk J Pediatr. 2004 Apr-Jun;46(2):137-41. Turk J Pediatr. 2004. PMID: 15214742 Clinical Trial.

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