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Class in John Lanchester’s Fiction

Anglistik, 2023, Vol.34 (1), p.165-175

Sandrock, K.

2023

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Border Narratives

Anglistik, 2023, Vol.34 (3), p.7-18

2023

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Bernard‐Soulier syndrome in Pakistan: Biochemical and molecular analyses leading to identification of a novel mutation in GP1BA

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.e18-e22

2018

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Septins, a novel group of GTP-binding proteins: relevance in hemostasis, neuropathology and oncogenesis

Klinische Padiatrie, 2009-05, Vol.221 (3), p.150

2009

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Patients with Bernard-Soulier syndrome and different severity of the bleeding phenotype

Blood cells, molecules, & diseases, 2017-09, Vol.67, p.69-74

2017

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Genetics of inherited platelet disorders

Hämostaseologie, 2014, Vol.34 (2), p.133-141

2014

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Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families

Klinische Padiatrie, 2012-04, Vol.224 (3), p.174-178

2012

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Reviews

Anglistik, 2020, Vol.31 (3), p.237-248

2020

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A large Swiss family with Bernard-Soulier syndrome - Correlation phenotype and genotype

Hämostaseologie, 2009-05, Vol.29 (2), p.161-167

2009

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Compound heterozygous mutations in 2 siblings with Hermansky-Pudlak syndrome type 1 (HPS1)

Klinische Padiatrie, 2010-05, Vol.222 (3), p.168-174

2010

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Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I

Klinische Padiatrie, 2010-05, Vol.222 (3), p.150

2010

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Two simple tools for industrial OR

Orion (Johannesburg, South Africa), 2003-12, Vol.3 (1)

Sandrock, K.

2003

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A TQC philosophy

Orion (Johannesburg, South Africa), 2003-12, Vol.7 (1)

Sandrock, K.

2003

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Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

Thrombosis and haemostasis, 2011-09, Vol.106 (3), p.475-483

2011

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Septins, a Novel Group of GTP-binding Proteins – Relevance in Hemostasis, Neuropathology and Oncogenesis

Klinische Pädiatrie, 2009-03, Vol.221 (3), p.150-155

2009

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In vitro generation of hiPSC-derived megakaryocytes and platelets from a patient with Glanzmann thrombasthenia

European heart journal, 2013-08, Vol.34 (suppl 1), p.5867-5867

2013

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n Vinnige en kragtige benadering tot kapitaalbeleggingsbesluitneming

Orion (Johannesburg, South Africa), 2003-12, Vol.2 (1)

2003

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Human endothelial and platelet septin SEPT11: cloning of novel variants and characterisation of interaction partners

Thrombosis and haemostasis, 2010-12, Vol.104 (6), p.1201-1210

2010

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Novel Homozygous Mutation (c.175delG) in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann's Thrombasthenia Type I

Klinische Pädiatrie, 2010-05, Vol.222 (3), p.150-153

2010

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Bernard‐Soulier syndrome in Pakistan: Biochemical and molecular analyses leading to identification of a novel mutation in GP 1 BA

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1)

2018

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Some thoughts on systems in management

South African journal of business management, 1979-03, Vol.10 (1), p.17-21

Sandrock, K.

1979

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A Simple Algorithm for Solving Small, Fixed-Charge Transportation Problems

The Journal of the Operational Research Society, 1988-05, Vol.39 (5), p.467-475

Sandrock, Keith

1988

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Heuristic estimation of pedestrian traffic volumes

Transportation research. Part A: general, 1988-03, Vol.22 (2), p.89-95

Sandrock, Keith

1988

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Metabolic fate of the thrombolytic agent benzarone in man: comparison with the rat and dog

Xenobiotica, 1987, Vol.17 (7), p.881-896

1987

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Causes of variation of copper, iron, manganese, zinc and magnesium levels in bovine livers. 3. The effects of locality

Journal of the South African Veterinary Association, 1975-09, Vol.46 (3), p.249

1975

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Class in John Lanchester’s Fiction

Border Narratives

Bernard‐Soulier syndrome in Pakistan: Biochemical and molecular analyses leading to identification of a novel mutation in GP1BA

Septins, a novel group of GTP-binding proteins: relevance in hemostasis, neuropathology and oncogenesis

Patients with Bernard-Soulier syndrome and different severity of the bleeding phenotype

Genetics of inherited platelet disorders

Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families

Reviews

A large Swiss family with Bernard-Soulier syndrome - Correlation phenotype and genotype

Compound heterozygous mutations in 2 siblings with Hermansky-Pudlak syndrome type 1 (HPS1)

Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I

Two simple tools for industrial OR

A TQC philosophy

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

Septins, a Novel Group of GTP-binding Proteins – Relevance in Hemostasis, Neuropathology and Oncogenesis

In vitro generation of hiPSC-derived megakaryocytes and platelets from a patient with Glanzmann thrombasthenia

n Vinnige en kragtige benadering tot kapitaalbeleggingsbesluitneming

Human endothelial and platelet septin SEPT11: cloning of novel variants and characterisation of interaction partners

Novel Homozygous Mutation (c.175delG) in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann's Thrombasthenia Type I

Bernard‐Soulier syndrome in Pakistan: Biochemical and molecular analyses leading to identification of a novel mutation in GP 1 BA

Some thoughts on systems in management

A Simple Algorithm for Solving Small, Fixed-Charge Transportation Problems

Heuristic estimation of pedestrian traffic volumes

Metabolic fate of the thrombolytic agent benzarone in man: comparison with the rat and dog

Causes of variation of copper, iron, manganese, zinc and magnesium levels in bovine livers. 3. The effects of locality

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