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Critical incident reporting in the intensive care unit

Anaesthesia, 1997-05, Vol.52 (5), p.403-409

1997

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Long-term outcome and functional health status following intensive care in Hong Kong

Critical care medicine, 1999-01, Vol.27 (1), p.51-57

1999

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Recovery after propofol infusion anaesthesia in children : comparison with propofol, thiopentone of halothane induction followed by halothane maintenance

British journal of anaesthesia : BJA, 1994-05, Vol.72 (5), p.554-558

1994

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Ondansetron 4 mg for the prevention of nausea and vomiting after minor laparoscopic gynaecological surgery

Anaesthesia and intensive care, 1994-04, Vol.22 (2), p.142-146

1994

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Recovery after propofol infusion anaesthesia in children: comparision with propofol, thiopentone or halothane induction followed by halothane maintenance

British journal of anaesthesia : BJA, 1994-05, Vol.72 (5), p.554-558

1994

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Translation and calibration of a Chinese version of the Sickness Impact Profile for use in Hong Kong

Hong Kong medical journal = Xianggang yi xue za zhi, 1998-12, Vol.4 (4), p.375-381

1998

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Recovery after Propofol Infusion Anesthesia in Children: Comparison with Propofol, Thiopentone or Halothane Induction Followed by Halothane Maintenance

Survey of anesthesiology, 1995-02, Vol.39 (1), p.54

1995

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Ondansetron mg for the prevention of nausea and vomiting after minor laparoscopic gynaecological surgery

Anaesthesia and intensive care, 1994, Vol.22 (2), p.142-146

1994

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Radiotherapy treatment planning of prostate cancer using magnetic resonance imaging alone

Radiotherapy and oncology, 2003-02, Vol.66 (2), p.203-216

2003

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3-[(2R)-Amino-2-phenylethyl]-1-(2,6-difluorobenzyl)-5-(2-fluoro-3-methoxyphenyl)- 6-methylpyrimidin-2,4-dione (NBI 42902) as a Potent and Orally Active Antagonist of the Human Gonadotropin-Releasing Hormone Receptor. Design, Synthesis, and in Vitro and in Vivo Characterization

Journal of medicinal chemistry, 2005-02, Vol.48 (4), p.1169-1178

2005

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Synthesis and Structure−Activity Relationships of 1-Arylmethyl-5-aryl-6-methyluracils as Potent Gonadotropin-Releasing Hormone Receptor Antagonists

Journal of medicinal chemistry, 2004-02, Vol.47 (5), p.1259-1271

2004

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Pharmacokinetic characterization of a natural product–inspired novel MEK1 inhibitor E6201 in preclinical species

Cancer chemotherapy and pharmacology, 2012, Vol.69 (1), p.229-237

2012

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3-(2-Aminoalkyl)-1-(2,6-difluorobenzyl)-5- (2-fluoro-3-methoxyphenyl)-6-methyl- uracils as Orally Bioavailable Antagonists of the Human Gonadotropin Releasing Hormone Receptor

Journal of medicinal chemistry, 2004-07, Vol.47 (14), p.3483-3486

2004

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Uracils as potent antagonists of the human gonadotropin-releasing hormone receptor without atropisomers

Bioorganic & medicinal chemistry letters, 2005-05, Vol.15 (10), p.2519-2522

2005

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Structure–activity relationships of 1,3,5-triazine-2,4,6-triones as human gonadotropin-releasing hormone receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (16), p.3685-3690

2005

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Synthesis and structure–activity relationships of uracil derived human GnRH receptor antagonists: ( R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5

Bioorganic & medicinal chemistry letters, 2004-10, Vol.14 (19), p.4967-4973

2004

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Routine preoperative screening for human immunodeficiency virus in a general hospital, Saudi Arabia

Infection control and hospital epidemiology, 1997-03, Vol.18 (3), p.158-159

1997

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Routine Preoperative Screening for Human Immunodeficiency Virus in a General Hospital, Saudi Arabia

Infection control and hospital epidemiology, 1997-03, Vol.18 (3), p.158-159

1997

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Potent imidazole and triazole CB 1 receptor antagonists related to SR141716

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (5), p.1151-1154

2004

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ChemInform Abstract: Crystal and Molecular Structure and Spectra of K4(Ni(NO2)6)×H2O and K3(Ni(NO2)4(O2N))

ChemInform, 1994-05, Vol.25 (21), p.no-no

1994

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Critical incident reporting in the intensive care unit

Long-term outcome and functional health status following intensive care in Hong Kong

Recovery after propofol infusion anaesthesia in children : comparison with propofol, thiopentone of halothane induction followed by halothane maintenance

Ondansetron 4 mg for the prevention of nausea and vomiting after minor laparoscopic gynaecological surgery

Recovery after propofol infusion anaesthesia in children: comparision with propofol, thiopentone or halothane induction followed by halothane maintenance

Translation and calibration of a Chinese version of the Sickness Impact Profile for use in Hong Kong

Recovery after Propofol Infusion Anesthesia in Children: Comparison with Propofol, Thiopentone or Halothane Induction Followed by Halothane Maintenance

Ondansetron mg for the prevention of nausea and vomiting after minor laparoscopic gynaecological surgery

Radiotherapy treatment planning of prostate cancer using magnetic resonance imaging alone

3-[(2R)-Amino-2-phenylethyl]-1-(2,6-difluorobenzyl)-5-(2-fluoro-3-methoxyphenyl)- 6-methylpyrimidin-2,4-dione (NBI 42902) as a Potent and Orally Active Antagonist of the Human Gonadotropin-Releasing Hormone Receptor. Design, Synthesis, and in Vitro and in Vivo Characterization

Synthesis and Structure−Activity Relationships of 1-Arylmethyl-5-aryl-6-methyluracils as Potent Gonadotropin-Releasing Hormone Receptor Antagonists

Pharmacokinetic characterization of a natural product–inspired novel MEK1 inhibitor E6201 in preclinical species

3-(2-Aminoalkyl)-1-(2,6-difluorobenzyl)-5- (2-fluoro-3-methoxyphenyl)-6-methyl- uracils as Orally Bioavailable Antagonists of the Human Gonadotropin Releasing Hormone Receptor

Uracils as potent antagonists of the human gonadotropin-releasing hormone receptor without atropisomers

Structure–activity relationships of 1,3,5-triazine-2,4,6-triones as human gonadotropin-releasing hormone receptor antagonists

Synthesis and structure–activity relationships of uracil derived human GnRH receptor antagonists: ( R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5

Routine preoperative screening for human immunodeficiency virus in a general hospital, Saudi Arabia

Routine Preoperative Screening for Human Immunodeficiency Virus in a General Hospital, Saudi Arabia

Potent imidazole and triazole CB 1 receptor antagonists related to SR141716

ChemInform Abstract: Crystal and Molecular Structure and Spectra of K4(Ni(NO2)6)×H2O and K3(Ni(NO2)4(O2N))

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