Cağlar M - Search Results

1

Cerebrospinal fluid glutamine level in the differential diagnosis of a "bloody tap" in newborn infants.

Yurdakök M, Göktoğan S, Erdem G, Ozalp I, Tekinalp G, Coşkun T, Cağlar M. Yurdakök M, et al. Among authors: caglar m. Brain Dev. 1992 Nov;14(6):428-9. doi: 10.1016/s0387-7604(12)80357-3. Brain Dev. 1992. PMID: 1492661 No abstract available.

2

A case of Pearson syndrome associated with multiple renal cysts.

Gürgey A, Ozalp I, Rötig A, Coşkun T, Tekinalp G, Erdem G, Akeören Z, Caglar M, Bakkaloglu A. Gürgey A, et al. Among authors: caglar m. Pediatr Nephrol. 1996 Oct;10(5):637-8. doi: 10.1007/s004670050178. Pediatr Nephrol. 1996. PMID: 8897573

3

Type I hereditary tyrosinaemia: presentation of 11 cases.

Coşkun T, Ozalp I, Koçak N, Yüce A, Caglar M, Berger R. Coşkun T, et al. Among authors: caglar m. J Inherit Metab Dis. 1991;14(5):765-70. doi: 10.1007/BF01799947. J Inherit Metab Dis. 1991. PMID: 1664010

4

I-cell disease. A case report and review of the literature.

Güngör N, Coşkun T, Akçören Z, Cağlar M. Güngör N, et al. Among authors: caglar m. Turk J Pediatr. 1994 Apr-Jun;36(2):145-52. Turk J Pediatr. 1994. PMID: 8016916

5

Placental apoptosis in pregnancies with intrauterine meconium passage.

Korkmaz A, Tekinalp G, Oran O, Yurdakök M, Yiğit S, Cağlar M, Akçören Z, Onderoğlu L, Uçkan D. Korkmaz A, et al. Among authors: caglar m. Am J Perinatol. 2005 Apr;22(3):133-8. doi: 10.1055/s-2005-863788. Am J Perinatol. 2005. PMID: 15838746

6

Neonatal form of hypophosphatasia. A case report.

Tekinalp G, Gürakan B, Yalçin S, Cağlar M, Ergin H. Tekinalp G, et al. Among authors: caglar m. Turk J Pediatr. 1995 Oct-Dec;37(4):421-4. Turk J Pediatr. 1995. PMID: 8560613

7

Hepatic mucormycosis in a child with fulminant hepatic failure.

Erdem G, Cağlar M, Ceyhan M, Akçören Z, Kanra G. Erdem G, et al. Among authors: caglar m. Turk J Pediatr. 1996 Oct-Dec;38(4):511-4. Turk J Pediatr. 1996. PMID: 8993182

8

Preoperative use of octreotide in a newborn with persistent hyperinsulinemic hypoglycemia of infancy.

Apak RA, Yurdakök M, Oran O, Senocak ME, Cağlar M. Apak RA, et al. Among authors: caglar m. J Pediatr Endocrinol Metab. 1998 Mar;11 Suppl 1:143-5. doi: 10.1515/jpem.1998.11.s1.143. J Pediatr Endocrinol Metab. 1998. PMID: 9642652

9

A case with early infantile form of galactosialidosis with unusual haematological findings.

Tekinalp G, Aliefendioğlu D, Yüce A, Cağlar M, Beck M. Tekinalp G, et al. Among authors: caglar m. J Inherit Metab Dis. 1999 Jun;22(5):668-9. doi: 10.1023/a:1005598517882. J Inherit Metab Dis. 1999. PMID: 10399101 No abstract available.

10

The triad of nesidioblastosis, congenital neuroblastoma and glomerulocystic disease of the newborn: a case report.

Bulun A, Sarici SU, Soyer OU, Tekşam O, Yurdakök M, Cağlar M. Bulun A, et al. Among authors: caglar m. Turk J Pediatr. 2005 Jul-Sep;47(3):298-302. Turk J Pediatr. 2005. PMID: 16250322

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