Berkel AI - Search Results

1

Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey.

Berkel AI, Birben E, Oner C, Oner R, Loos M, Petry F. Berkel AI, et al. Immunobiology. 2000 Jan;201(3-4):347-55. doi: 10.1016/S0171-2985(00)80089-3. Immunobiology. 2000. PMID: 10776791

2

Development of systemic lupus erythematosus in a patient with selective complete C1q deficiency.

Berkel AI, Petry F, Sanal O, Tinaztepe K, Ersoy F, Bakkaloglu A, Loos M. Berkel AI, et al. Eur J Pediatr. 1997 Feb;156(2):113-5. doi: 10.1007/s004310050567. Eur J Pediatr. 1997. PMID: 9039514

3

Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis.

Petry F, Berkel AI, Loos M. Petry F, et al. Among authors: berkel ai. Hum Genet. 1997 Jul;100(1):51-6. doi: 10.1007/s004390050464. Hum Genet. 1997. PMID: 9225968

4

Clinical and immunological studies in a case of selective complete C1q deficiency.

Berkel AI, Loos M, Sanal O, Mauff G, Güngen Y, Ors U, Ersoy F, Yegin O. Berkel AI, et al. Clin Exp Immunol. 1979 Oct;38(1):52-63. Clin Exp Immunol. 1979. PMID: 527255 Free PMC article.

5

[Clinical findings in children with selective deficiency of Clq, a subunit of the first component of complement].

Berkel AI, Loos M. Berkel AI, et al. Monatsschr Kinderheilkd. 1983 Mar;131(3):161-5. Monatsschr Kinderheilkd. 1983. PMID: 6855782 German.

6

Studies of immune response in a patient with selective complete C1q deficiency.

Berkel AI. Berkel AI. Turk J Pediatr. 1993 Jul-Sep;35(3):221-6. Turk J Pediatr. 1993. PMID: 8165758

7

Immunochemical and functional analysis of a complete C1q deficiency in man: evidence that C1r and C1s are in the native form, and that they reassociate with purified C1q to form macromolecular C1.

Loos M, Laurell AB, Sjöholm AG, Mårtensson U, Berkel AI. Loos M, et al. Among authors: berkel ai. J Immunol. 1980 Jan;124(1):59-63. J Immunol. 1980. PMID: 7350234 No abstract available.

8

Homozygous C2 deficiency: association with defective alternative pathway function and immunoglobulin deficiency.

Sanal O, Yel L, Tezcan I, Ersoy F, Berkel AI. Sanal O, et al. Among authors: berkel ai. Int Arch Allergy Immunol. 1996 Jun;110(2):195-8. doi: 10.1159/000237287. Int Arch Allergy Immunol. 1996. PMID: 8645999

9

Selective IgA deficiency with unusual features: development of common variable immunodeficiency, Sjögren's syndrome, autoimmune hemolytic anemia and immune thrombocytopenic purpura.

Sanal O, Ersoy F, Metin A, Tezcan I, Berkel AI, Yel L. Sanal O, et al. Among authors: berkel ai. Acta Paediatr Jpn. 1995 Aug;37(4):526-9. doi: 10.1111/j.1442-200x.1995.tb03369.x. Acta Paediatr Jpn. 1995. PMID: 7572159

10

Polymorphism of the fourth component of complement in Turks.

Metin A, Sanal O, Ersoy F, Tezcan I, Berkel AI, Irkeç C. Metin A, et al. Among authors: berkel ai. Hum Biol. 2000 Jun;72(3):527-33. Hum Biol. 2000. PMID: 10885198

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