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025 The utility of nerve blood flow in the assessment of peripheral neuropathy

Journal of neurology, neurosurgery and psychiatry, 2019-07, Vol.90 (e7), p.A9-A9

2019

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06.03 Integrative analysis of neuroblastoma by single-cell RNA sequencing identifies the NECTIN2-TIGIT axis as a target for immunotherapy

Journal for immunotherapy of cancer, 2022-09, Vol.10 (Suppl 1), p.A2-A2

2022

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OS 06-09 THE SYNERGISTIC ASSOCIATION BETWEEN VITAMIN D AND VITAMIN K WITH INCIDENT HYPERTENSION

Journal of hypertension, 2016-09, Vol.34 Suppl 1 - ISH 2016 Abstract Book (Supplement 1), p.e64-e64

2016

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0D Model for the Comparative Analysis of Hydrogen Carriers in Ship’s Integrated Energy Systems

Modelling and Optimisation of Ship Energy Systems 2023, 2024-01

2024

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1-02-07 Present health conditions and functional status of a population based cohort of the 1956 poliomyelitis outbreak in Holland

Journal of the neurological sciences, 1997-09, Vol.150, p.S5-S5

1997

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1,1,1,5,5,5-Hexafluoro-2,4-dimeth-oxy-pentane-2,4-diol

Acta crystallographica. Section E, Structure reports online, 2011-12, Vol.67 (Pt 12), p.o3155-o3155

2011

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1,1,1,5,5,5-Hexafluoro-2,4-dimethoxypentane-2,4-diol

Acta crystallographica. Section E, Structure reports online, 2011-12, Vol.67 (12), p.o3155-o3155

2011

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1:1 Ground-track resonance in a uniformly rotating 4th degree and order gravitational field

Celestial mechanics and dynamical astronomy, 2017, Vol.127 (1), p.67-93

2017

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1.18 A versatile cryopump for industrial vacuum systems

Vacuum, 1977, Vol.27 (3), p.175-180

1977

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1-[ 18F]fluoro-2-propanol p-toluenesulfonate: a synthon for the preparation of N-([ 18F]fluoroisopropyl)amines

International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 1992, Vol.43 (11), p.1335-1339

1992

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. I, N-methyl-N-ethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide METM(TCNQ)2 and N-methyl-N-butyl-thiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBTM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990, Vol.46 (5), p.852-856

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. II, N-methyl-N-propylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MPM(TCNQ)2 and N-methyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990, Vol.46 (5), p.857-860

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. III, N-ethyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBM(TCNQ)2 and N-ethyl-N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBTM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990, Vol.46 (5), p.860-864

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. IV, N,N-dimethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide DMTM(TCNQ)2 at room temperature and its phase transition at 272 K

Acta crystallographica. Section C, Crystal structure communications, 1990, Vol.46 (5), p.864-866

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part I. N-Methyl-N-ethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide METM(TCNQ)2 and N-methyl-N-butyl-thiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBTM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.852-856

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part I. N-Methyl-N-ethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide METM(TCNQ)2 andN-methyl-N-butyl-thiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBTM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.852-856

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part II. N-Methyl-N-propylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MPM(TCNQ)2 and N-methyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.857-860

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part III. N-Ethyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBM(TCNQ)2 and N-ethyl-N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBTM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.860-864

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part IV. N,N-Dimethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide DMTM(TCNQ)2 at room temperature and its phase transition at 272 K

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.864-866

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part V. Average structure of N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HBTM(TCNQ)2and short-range ordering

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.867-869

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part VI. N-Methylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HMM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990-05, Vol.46 (5), p.869-871

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. V, Average structure of N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HBTM(TCNQ)2 and short-range ordering

Acta crystallographica. Section C, Crystal structure communications, 1990, Vol.46 (5), p.867-869

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. VI, N-methylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HMM(TCNQ)2

Acta crystallographica. Section C, Crystal structure communications, 1990, Vol.46 (5), p.869-871

1990

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1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. VII. Triclinic form of N,N-dimethylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide, DMM(TCNQ)2 (II), at 294 K

Acta crystallographica. Section C, Crystal structure communications, 1994-07, Vol.50 (7), p.1139-1141

1994

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1.2: Invited Paper: Creating a high quality optical experience for Augmented Reality Devices

SID International Symposium Digest of technical papers, 2022-10, Vol.53 (S1), p.42-42

2022

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025 The utility of nerve blood flow in the assessment of peripheral neuropathy

06.03 Integrative analysis of neuroblastoma by single-cell RNA sequencing identifies the NECTIN2-TIGIT axis as a target for immunotherapy

OS 06-09 THE SYNERGISTIC ASSOCIATION BETWEEN VITAMIN D AND VITAMIN K WITH INCIDENT HYPERTENSION

0D Model for the Comparative Analysis of Hydrogen Carriers in Ship’s Integrated Energy Systems

1-02-07 Present health conditions and functional status of a population based cohort of the 1956 poliomyelitis outbreak in Holland

1,1,1,5,5,5-Hexafluoro-2,4-dimeth-oxy-pentane-2,4-diol

1,1,1,5,5,5-Hexafluoro-2,4-dimethoxypentane-2,4-diol

1:1 Ground-track resonance in a uniformly rotating 4th degree and order gravitational field

1.18 A versatile cryopump for industrial vacuum systems

1-[ 18F]fluoro-2-propanol p-toluenesulfonate: a synthon for the preparation of N-([ 18F]fluoroisopropyl)amines

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. I, N-methyl-N-ethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide METM(TCNQ)2 and N-methyl-N-butyl-thiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBTM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. II, N-methyl-N-propylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MPM(TCNQ)2 and N-methyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. III, N-ethyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBM(TCNQ)2 and N-ethyl-N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBTM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. IV, N,N-dimethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide DMTM(TCNQ)2 at room temperature and its phase transition at 272 K

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part I. N-Methyl-N-ethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide METM(TCNQ)2 and N-methyl-N-butyl-thiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBTM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part I. N-Methyl-N-ethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide METM(TCNQ)2 andN-methyl-N-butyl-thiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBTM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part II. N-Methyl-N-propylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MPM(TCNQ)2 and N-methyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide MBM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part III. N-Ethyl-N-butylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBM(TCNQ)2 and N-ethyl-N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide EBTM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part IV. N,N-Dimethylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide DMTM(TCNQ)2 at room temperature and its phase transition at 272 K

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part V. Average structure of N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HBTM(TCNQ)2and short-range ordering

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. Part VI. N-Methylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HMM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. V, Average structure of N-butylthiomorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HBTM(TCNQ)2 and short-range ordering

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. VI, N-methylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide HMM(TCNQ)2

1:2 complexes of (thio)morpholinium derivatives and the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane. VII. Triclinic form of N,N-dimethylmorpholinium di-7,7,8,8-tetracyano-p-quinodimethanide, DMM(TCNQ)2 (II), at 294 K

1.2: Invited Paper: Creating a high quality optical experience for Augmented Reality Devices

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