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A new method for the determination of the mechanical properties of the vitreous

Ophthalmic research, 1982-01, Vol.14 (5), p.326-334

1982

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The mechanical properties of the vitreous of pig and human donor eyes

Ophthalmic research, 1982-01, Vol.14 (5), p.335-343

1982

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Impaired response to intrarenal administered atrial natriuretic peptide in ischemic acute renal failure of a transplanted patient

Mineral and electrolyte metabolism, 1990, Vol.16 (1), p.34

1990

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Prothrombin consumption, serum prothrombic activity and prothrombin conversion accelerator in hemophilia and thrombocytopenia

The Journal of clinical investigation, 1949-11, Vol.28 (6 Pt 2), p.1511-1516

1949

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Studies of thiamine metabolism in man; thiamine balance; the normal requirement of vitamin B1 and the role of fecal thiamine in human nutrition

The Journal of clinical investigation, 1946-05, Vol.25, p.287-293

1946

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Evolution of a prothrombin conversion accelerator in stored human plasma and prothrombin fractions

The American journal of physiology, 1949-11, Vol.159 (2), p.322-331

1949

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Thrombasthenia and thrombocytopenic purpura; report of case demonstrating qualitative and quantitative inadequacy of platelets

The New England journal of medicine, 1949-12, Vol.241 (24), p.965-968

1949

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The prothrombin conversion accelerator of serum (SPCA): its partial purification and its properties compared with serum AC-globulin

The Journal of clinical investigation, 1950-07, Vol.29 (7), p.881-895

1950

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The labile factor of prothrombin conversion: its consumption under normal and pathological conditions affecting blood coagulation

The Journal of clinical investigation, 1951-03, Vol.30 (3), p.252-262

1951

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Congenital SPCA deficiency: a hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions

The Journal of clinical investigation, 1951-06, Vol.30 (6), p.596-608

1951

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Studies of thiamine metabolism in man; thiamine and pyrimidine excretion with special reference to the relationship between injected and excreted thiamine in normal and abnormal subjects

The Journal of clinical investigation, 1946-05, Vol.25, p.294-303

1946

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Amniotic fluid analysis to improve fetal survival

The Journal of the Maine Medical Association, 1966-08, Vol.57 (8), p.163

1966

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A Prothrombin Conversion Accelerator in Serum

Science (American Association for the Advancement of Science), 1949-05, Vol.109 (2839), p.545-545

1949

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Studies of hemophilia; the assay of the antihemophilic clot-promoting principle in normal human plasma with some observations on the relative potency of certain plasma fractions

The Journal of clinical investigation, 1948-01, Vol.27 (1), p.98-105

1948

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Studies on hemophilia; the control of hemophilia by repeated infusions of normal human plasma

Journal of the American Medical Association, 1948-09, Vol.138 (3), p.174

1948

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Congenital hypoprothrombinemia: A case study with particular reference to the role of non-prothrombin factors in the conversion of prothrombin

The American journal of medicine, 1950-01, Vol.8 (2), p.255-259

1950

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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

Neurology, 2007-03, Vol.68 (10), p.743-750

2007

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Combined HILIC-ELSD/ESI-MS(n) enables the separation, identification and quantification of sugar beet pectin derived oligomers

Carbohydrate polymers, 2012-09, Vol.90 (1), p.41-48

2012

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Caldendrin-Jacob: a protein liaison that couples NMDA receptor signalling to the nucleus

PLoS biology, 2008-02, Vol.6 (2), p.e34-e34

2008

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T2 assessment and clinical outcome following autologous matrix-assisted chondrocyte and osteochondral autograft transplantation

Osteoarthritis and cartilage, 2009-12, Vol.17 (12), p.1576-1582

2009

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Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization

Nephrology, dialysis, transplantation, 2011-01, Vol.26 (1), p.136-143

2011

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Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4

Human molecular genetics, 2007-06, Vol.16 (12), p.1488-1494

2007

Volltextzugriff (PDF)

Comprehensive Characterization of Genomic Aberrations in Gangliogliomas by CGH, Array-based CGH and Interphase FISH

Brain pathology (Zurich, Switzerland), 2008-07, Vol.18 (3), p.326-337

2008

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Alignment does not influence cartilage T2 in asymptomatic knee joints

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2014-06, Vol.22 (6), p.1396-1403

2014

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Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis

Human genetics, 2013-07, Vol.132 (7), p.825-841

2013

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A new method for the determination of the mechanical properties of the vitreous

The mechanical properties of the vitreous of pig and human donor eyes

Impaired response to intrarenal administered atrial natriuretic peptide in ischemic acute renal failure of a transplanted patient

Prothrombin consumption, serum prothrombic activity and prothrombin conversion accelerator in hemophilia and thrombocytopenia

Studies of thiamine metabolism in man; thiamine balance; the normal requirement of vitamin B1 and the role of fecal thiamine in human nutrition

Evolution of a prothrombin conversion accelerator in stored human plasma and prothrombin fractions

Thrombasthenia and thrombocytopenic purpura; report of case demonstrating qualitative and quantitative inadequacy of platelets

The prothrombin conversion accelerator of serum (SPCA): its partial purification and its properties compared with serum AC-globulin

The labile factor of prothrombin conversion: its consumption under normal and pathological conditions affecting blood coagulation

Congenital SPCA deficiency: a hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions

Studies of thiamine metabolism in man; thiamine and pyrimidine excretion with special reference to the relationship between injected and excreted thiamine in normal and abnormal subjects

Amniotic fluid analysis to improve fetal survival

A Prothrombin Conversion Accelerator in Serum

Studies of hemophilia; the assay of the antihemophilic clot-promoting principle in normal human plasma with some observations on the relative potency of certain plasma fractions

Studies on hemophilia; the control of hemophilia by repeated infusions of normal human plasma

Congenital hypoprothrombinemia: A case study with particular reference to the role of non-prothrombin factors in the conversion of prothrombin

DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

Combined HILIC-ELSD/ESI-MS(n) enables the separation, identification and quantification of sugar beet pectin derived oligomers

Caldendrin-Jacob: a protein liaison that couples NMDA receptor signalling to the nucleus

T2 assessment and clinical outcome following autologous matrix-assisted chondrocyte and osteochondral autograft transplantation

Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization

Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4

Comprehensive Characterization of Genomic Aberrations in Gangliogliomas by CGH, Array-based CGH and Interphase FISH

Alignment does not influence cartilage T2 in asymptomatic knee joints

Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis

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