283 results on '"Schlammadinger A"'
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102. P061 Type 3 von Willebrand disease in Hungary: A partial large deletion is the most common genetic defect
103. COULD HEPARIN-INDUCED THROMBOCYTOPENIA AND THROMBOSIS BE A RARE MANIFESTATION OF ANTIPHOSPHOLIPID ANTIBODY SYNDROME?
104. The A/T1381 polymorphism in the A1-domain of von Willebrand factor influences the affinity of von Willebrand factor for platelet glycoprotein Ibα
105. Type 2B von Willebrand disease in seven individuals from three different families: Phenotypic and genotypic characterization
106. Low Molecular Weight Heparin as Thromboprophylaxis Throughout Pregnancy in Heritable Thrombophilic Women
107. Plasma glycocalicin as a source of GPIbα in the von Willebrand factor ristocetin cofactor ELISA
108. P052 Low dose factor concentrate prophylaxis in patients with severe haemorrhagic disorders
109. P050 Successful immune tolerance induction treatment of therapy-resistent acquired haemophilia with high inhibitor titer: a case report
110. Occurrence of the Asn45Ser mutation in the GPIX gene in a Belgian patient with Bernard Soulier syndrome
111. Fc-receptor Dependent Platelet Aggregation Induced by Monoclonal Antibodies against Platelet Glycoprotein Ib or von Willebrand Factor
112. Protease-elicited TUNEL Positivity of Non-apoptotic Fixed Cells
113. Use of a platelet filter test in patients with thrombocytosis
114. A Reliable and Reproducible ELISA Method to Measure Ristocetin Cofactor Activity of von Willebrand Factor
115. Comparison of the O’Brien Filter Test and the PFA-100 Platelet Analyzer in the Laboratory Diagnosis of von Willebrand’s Disease
116. Comparison of PFA-100 Closure Time and Template Bleeding Time of Patients with Inherited Disorders Causing Defective Platelet Function
117. Acquired Bernard-Soulier Syndrome: A Case with Necrotizing Vasculitis and Thrombosis
118. Different effects of an oligonucleotide uptake stimulating protein on leukemic cells in their primitive and differentiated state
119. DNA uptake stimulating protein from Neurospora crassa enhances DNA and oligonucleotide uptake also in mammalian cells
120. Anticytoskeletal antibodies in systemic autoimmune diseases
121. Systemic Sclerosis and Exposure to Trichloroethylene
122. Signs of systemic disease in localized scleroderma
123. Anticentromere Antibody and Raynaud’s Phenomenon
124. A new approach to chromosome scaffold studies
125. Systemic Sclerosis and Exposure to Trichloroethylene
126. Signs of systemic disease in localized scleroderma
127. Anticentromere Antibody and Raynaud’s Phenomenon
128. A new approach to chromosome scaffold studies
129. Common large partial VWFgene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population
130. X-Linked Recessive Ichthyosis.
131. Progressive Systemic Sclerosis Occurring in Patients Exposed to Chemicals.
132. Combination of fluorescence in situ hybridization and scanning force microscopy for the ultrastructural characterization of defined chromatin regions.
133. Plasma glycocalicin as a source of GPIbα in the von Willebrand factor ristocetin cofactor ELISA
134. Über gedrehte Haare, Pili torti.
135. Phytogene Hauterkrankungen, mit besonderer Rücksicht auf die Wiesendermatitis.
136. Inhibition of the development of Q-bands on human chromosomes by netropsin
137. X-Linked Recessive Ichthyosis
138. A Reliable and Reproducible ELISA Method to Measure Ristocetin Cofactor Activity of von Willebrand Factor
139. Contents, Vol. 67, 1933
140. Cylindrom und Trichoepithelioma papulosum multiplex
141. Über gedrehte Haare, Pili torti
142. Selected problems and prospects of high-speed cell analysis
143. [Letter: Automation of laboratory tests]
144. [Questions of principle in genetics]
145. [Thoughts on genetics]
146. [Follow-up studies in a family with ichthyosis vulgaris]
147. [Important of nation-wide registration of genetic abnormalities]
148. The effect of Ro 20-1724 upon induced beta-galactosidase synthesis in Escherichia coli
149. The effect of quinacrine on the expression of lac operon in Escherichia coli promoter mutants
150. [On the Groenblad-Strandberg syndrome]
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