Ara
Toplam kayıt 82, listelenen: 21-40
Penetration of Topical, Oral, and Combined Administered Ofloxacin into the Subretinal Fluid
(Bmj Publishing Group, 1999)
Aims-To assess the subretinal fluid (SRF) levels of ofloxacin following topical, oral or combined administration. Methods-31 patients undergoing conventional retinal reattachment surgery were randomly assigned to three ...
Splicing Defects In The Ataxia-Telangiectasia Gene, Atm: Underlying Mutations And Consequences
(Cell Press, 1999)
Mutations resulting in defective splicing constitute a significant proportion (30/62 [48%]) of a new series of mutations in the ATM gene in patients with ataxia-telangiectasia (AT) that were detected by the protein-truncation ...
Kütüphanelerarası İşbirliğinin Neresindeyiz?
(TKD, 1999)
The amount of information sources available through both printed and
electronic media are ever increasing. Even libraries with considerable
collection development budgets are having difficulties in coping with
this ...
Tıp ve Yaşam Bilimleri Literatürüne Türkiye'nin Katkısı (1988-1997)
(TKD, 1999)
The contribution of Turkey to positive sciences is increasing. Turkish
scientists published more than 5.100 articles in scientific journals
indexed by the Institute for Scientific Information’s Science Citation
Index, ...
Crystal Structure Of 1-Ethyl-3-Methylbenzimidazole-2-Thione
(Japan Soc Analytical Chemistry, 1999)
Yazma katalogları ve TÜYATOK: Sorunlar ve çözüm önerileri
(Türk Kütüphaneciler Derneği, 1999)
Bis{(Mu-Nitrato)[Mu-Bis(Salicylidene)-1,3-Propanediaminato] Copper(II)}Zinc(II)
(Munksgaard Int Publ Ltd, 1999)
The title compound, [Zn{Cu(NO3)(C17H16N2O2)}(2)], has the central Zn2+ ion located on an inversion centre, with four bridging O atoms from two N,N'-bis(salicylidene)-1,3-propanediaminate (SALPD(2-)) ligands and one O atom ...
Attractors For The Generalized Benjamin-Bona-Mahony Equation
(Academic Press Inc, 1999)
We consider the periodic initial-boundary value problem for a multidimensional generalized Benjamin-Bona-Mahony equation. We show the existence of the global attractor with a finite Fractal dimension and the existence of ...
Crystal Structure Of 1,4 : 5,8-Dimethano-1,1A,4,4A,5,5A,8,8A-Octahydro-Anthracene-9,10-Dione, C16H16O2
(R Oldenbourg Verlag, 1999)
C16H16O2, monoclinic, P12(1)/n1 (No, 14), a = 12.0005(7) Angstrom, b = 6.2388(9) Angstrom, c = 16.973(2) Angstrom, beta = 110.609(6)degrees, V = 1189.5 Angstrom(3), Z = 4, R-gt(F) = 0.047, R-w(F-2) = 0.108, T = 293 K.
Crystal Structure Of 1,3-Dimethylbenzimidazole-2-Selenone, C9H10N2Se
(Walter De Gruyter Gmbh, 1999)
Seasonal Distribution of Large Phytoplankton in the Keban Dam Reservoir
(Oxford Univ Press, 1999)
The Keban Dam Reservoir (KDR), in eastern Anatolia, is one of the largest man-made reservoirs of the world with a storage capacity of >30 billion m(3). In the KDR, long-term water quality surveys have been carried out in ...
Wilms' Tumour-Associated Late Nephrotic Syndrome Responsive To Treatment
(Oxford Univ Press, 1999)
Serum Malondialdehyde Concentration in Babies with Hyperbilirubinaemia
(British Med Journal Publ Group, 1999)
Aim-To determine lipid peroxide concentrations in the first 10 days of life. Methods-Malondialdehyde concentrations were investigated in neonates with or without hyperbilirubinaemia during the first 10 days of life. ...
The Fanconi Anemia Group E Gene, Fance, Maps to Chromosome 6P
(Univ Chicago Press, 1999)
Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive disease with bone marrow failure and predisposition to cancer as major features, often accompanied by developmental anomalies. The cells of patients ...
A Characterization of Prime Submodules
(Academic Press Inc, 1999)
A Novel Protein Tyrosine Phosphatase Gene is Mutated in Progressive Myoclonus Epilepsy of the Lafora Type (Epm2)
(Oxford Univ Press, 1999)
Progressive myoclonus epilepsy of the Lafora type or Lafora disease (EPM2; McKusick no. 254780) is an autosomal recessive disorder characterized by epilepsy, myoclonus, progressive neurological deterioration and glycogen-like ...
A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9Q34
(Endocrine Soc, 1999)
Congenital generalized lipodystrophy (CGL, Berardinelli-Seip Syndrome, OMIM # 269700) is a rare autosomal recessive disorder characterized by near complete absence of adipose tissue from birth. Affected individuals have ...