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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A novel nonsense mutation in cathepsin C gene in an Egyptian patient presenting with Papillon–Lefèvre syndrome Soliman, Hala
2015
16 4 p. 387-392
6 p.
artikel
2 An overview on hepatitis C virus genotypes and its control Nouroz, Faisal
2015
16 4 p. 291-298
8 p.
artikel
3 Association of glutathione-S-transferase P1 (GSTP1)-313 A > G gene polymorphism and susceptibility to endometrial hyperplasia among Egyptian women Elsaid, Afaf
2015
16 4 p. 361-365
5 p.
artikel
4 Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient Shawky, Rabah M.
2015
16 4 p. 381-385
5 p.
artikel
5 Cancer ameliorating potential of Phyllanthus amarus: In vivo and in vitro studies against Aflatoxin B1 toxicity Ahmad, Md. Sultan
2015
16 4 p. 343-353
11 p.
artikel
6 Clinical application of sensory integration therapy for children with autism Alwi, Nazurah
2015
16 4 p. 393-394
2 p.
artikel
7 Differential response of biochemical parameters to EMS and MMS treatments and their dose effect relationship on chromosomes in induced diabetic mouse Khalandar, B.B.D.
2015
16 4 p. 301-312
12 p.
artikel
8 Editorial Board 2015
16 4 p. iii-
1 p.
artikel
9 Effectiveness of sensory integration program in motor skills in children with autism Abdel Karim, Amel E.
2015
16 4 p. 375-380
6 p.
artikel
10 Lipoprotein lipase gene variants: Association with acute myocardial infarction and lipid profiles Bahrami, Mahyar
2015
16 4 p. 327-332
6 p.
artikel
11 Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype Zaki, Moushira
2015
16 4 p. 367-374
8 p.
artikel
12 Patatin-like phospholipase domain containing-3 gene (PNPLA3) I148M polymorphism and liver damage in chronic hepatitis C Egyptian patients Mackawy, Amal M.H.
2015
16 4 p. 333-341
9 p.
artikel
13 Radioactive fallout and neural tube defects Akar, Nejat
2015
16 4 p. 299-300
2 p.
artikel
14 Rhodopsin mutations are scarcely implicated in autosomal recessive retinitis pigmentosa: A preliminary study of Egyptian retinitis pigmentosa patients Mebed, Reem
2015
16 4 p. 355-359
5 p.
artikel
15 The relation between antihistamine medication during early pregnancy & birth defects Shawky, Rabah M.
2015
16 4 p. 287-290
4 p.
artikel
16 The role of microRNAs on angiogenesis and vascular pressure in preeclampsia: The evidence from systematic review Harapan, Harapan
2015
16 4 p. 313-325
13 p.
artikel
                             16 gevonden resultaten
 
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