Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add more filters










Database
Language
Publication year range
1.
Pediatrics ; 113(2): e146-9, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14754985

ABSTRACT

A novel coronavirus-associated communicable respiratory disease, severe acute respiratory syndrome (SARS), spread worldwide after an outbreak in Guangdong Province of the People's Republic of China in November 2002. Since late February 2003, there has been an epidemic in Hong Kong involving both adult and pediatric patients. The clinical course, intensive care, and outcome of adolescent twin sisters with SARS are described. Adolescents infected with SARS may develop severe illness as adults, and close monitoring for disease progression in terms of both clinical and radiologic deterioration is warranted.


Subject(s)
Diseases in Twins , Severe Acute Respiratory Syndrome/physiopathology , Adolescent , Female , Humans , Lung/diagnostic imaging , Radiography , Severe acute respiratory syndrome-related coronavirus/isolation & purification , Severe Acute Respiratory Syndrome/diagnostic imaging
2.
Hong Kong Med J ; 10(1): 22-7, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14967851

ABSTRACT

OBJECTIVE: To estimate the incidence and document the clinical characteristics of Williams-Beuren syndrome in the Hong Kong Chinese population. DESIGN: Cytogenetic analysis and retrospective study. SETTING: Clinical Genetic Service, Department of Health, Hong Kong. PATIENTS: Forty-one Chinese patients with Williams-Beuren syndrome. MAIN OUTCOME MEASURES: From 1 January 1995 to 30 June 2002, fluorescence in situ hybridisation was used to confirm diagnoses in 41 cases of Williams-Beuren syndrome by detecting chromosome 7q microdeletion. Case records were reviewed, the incidence of the condition in the local population was estimated, and the main clinical characteristics were determined. RESULTS: The minimal incidence of Williams-Beuren syndrome in this locality was estimated to be approximately 1 per 23500 live births. Common dysmorphic facial features included periorbital fullness (83%), full lips (80%), a long philtrum (51%), a flat nasal bridge (41%), and abnormal teeth (37%). No patients had a stellate iris. The majority (82%) had at least one documented cardiac anomaly; among these patients, peripheral pulmonary stenosis was diagnosed in 61% and supravalvular aortic stenosis in 45%. Nearly all (93%) of the study group exhibited developmental delay. CONCLUSION: As in the West, patients with Williams-Beuren syndrome in the Hong Kong Chinese population display craniofacial dysmorphism, cardiovascular anomalies, and mental deficiency. Supravalvular aortic stenosis-the cardiac defect most commonly associated with Williams-Beuren syndrome in western countries-is less common than peripheral pulmonary stenosis in this region. Studies involving periodic cardiovascular evaluation are needed to confirm if this difference is significant.


Subject(s)
Williams Syndrome/epidemiology , Adolescent , Aortic Stenosis, Supravalvular/epidemiology , Aortic Stenosis, Supravalvular/genetics , Child , Child, Preschool , Chromosome Aberrations , Craniofacial Abnormalities/epidemiology , Craniofacial Abnormalities/genetics , Developmental Disabilities/epidemiology , Developmental Disabilities/genetics , Family , Female , Genetic Testing , Growth Disorders/epidemiology , Growth Disorders/genetics , Hong Kong/epidemiology , Humans , Hypercalcemia/epidemiology , Hypercalcemia/genetics , Incidence , Infant , Infant, Newborn , Male , Pulmonary Valve Stenosis/epidemiology , Pulmonary Valve Stenosis/genetics , Retrospective Studies , Williams Syndrome/genetics
3.
Dig Dis Sci ; 46(9): 1943-51, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11575447

ABSTRACT

Gastric infection with Helicobacter pylori results in chronic active gastritis and in some individuals is associated with complications such as peptic ulceration and gastric cancers. A balance between bacterial factors and host responses may determine disease outcome. The mouse-adapted H. pylori strain SS1 has been utilized as a model to study disease pathogenesis. Although chronic gastritis is observed in this murine model of H. pylori infection, other complications of disease seen in the human host (such as peptic ulceration) are not identified. The objectives of this study were to characterize virulence factors of the mouse-adapted H. pylori strain SS1 and determine host responses to infection. Vacuolating cytotoxin activity of H. pylori strain SS1 was determined after incubation of HEp-2 cells with culture supernatant for 24 hr. Polymerase chain reaction was performed to detect the presence of the cagA and cagE genes. Chemokine responses from human gastric epithelial cells infected with H. pylori SS1 were assessed by measurement of the concentration of interleukin-8 in cell-free supernatants. C57BL/6 and gld mice were infected with strain SS1 or sham-infected. Eight weeks following infection, gastric tissues were obtained for histological analysis and surface hydrophobicity was measured by axisymmetric drop-shape analysis. H. pylori strain SS1 was cytotoxin negative, cagA positive, and cagE positive, but induced only a modest interleukin-8 response (684 +/- 140 pg/ml) from AGS gastric epithelial cells in comparison to a clinical isolate (4170 +/- 410 pg/ml, P < 0.0005). Increased inflammation was observed in the stomachs of H. pylori strain SS1-infected animals compared to uninfected controls. Gastritis was not associated with any disease complications. Despite mucosal inflammation, infected mice did not demonstrate alterations in gastric surface hydrophobicity (42.2 degrees +/- 2.2 degrees and 41.4 degrees +/- 3.2 degrees for C57BL/6 and gld, respectively) compared to uninfected mice (43.2 degrees +/- 2.3 degrees and 39.5 degrees +/- 1.6 degrees, respectively). In conclusion, murine infection with H. pylori SS1, which contains putative bacterial virulence factors, results in gastric inflammation. However, the mucosal changes are not associated with alterations in surface hydrophobicity. Therefore, the mouse model of infection with H. pylori, strain SS1 may not serve as an entirely appropriate model to study host factors associated with disease complications.


Subject(s)
Antigens, Bacterial , Disease Models, Animal , Gastritis/microbiology , Helicobacter Infections/immunology , Helicobacter pylori , Animals , Bacterial Proteins/immunology , Bacterial Toxins/immunology , Cytotoxicity, Immunologic , Female , Gastric Mucosa/immunology , Gastritis/immunology , Helicobacter pylori/classification , Helicobacter pylori/genetics , Helicobacter pylori/immunology , Helicobacter pylori/pathogenicity , Humans , Mice , Mice, Inbred C57BL , Species Specificity , Virulence
4.
Anal Biochem ; 278(1): 14-21, 2000 Feb 01.
Article in English | MEDLINE | ID: mdl-10640348

ABSTRACT

A method for quantifying an intramolecularly linked all-d-amino acid peptide, NR58-3.14.3, in rat serum by LC-MS using selected ion monitoring with inclusion of a diastereomer as internal standard was developed. The reproducible quantitation of multiply charged compounds by LC-MS using single ion or selective reaction monitoring is often a challenge as the intensity ratio of the ions in a series of different charge states can vary. Good precision was obtained in the selected ion monitoring mode by integrating the summed ion currents of the singly, doubly, and triply charged molecular ions. Since stable isotope analogs are costly and integration of residual unlabeled material can be of concern, a diastereomer of NR58-3.14.3, NR58-3.14.5, was used as internal standard. The diastereomers were indistinguishable by electrospray MS, but fully separated by reversed-phase LC. Consequently, interference due to isotopic impurities or coelution was not encountered. The calibration plot was linear throughout a concentration range of 0.2 to 200.0 microg/ml (r(2) = 0.9996). Intraday precision of the standards analyzed was less than 12% RSD over the calibration range and the accuracy within +/-11% RE. Serum pharmacokinetics were in good agreement with the pharmacokinetic profiles of small, ionic, and polar molecules.


Subject(s)
Chemokine CCL2/analogs & derivatives , Peptides, Cyclic/blood , Animals , Chromatography, High Pressure Liquid/methods , Chromatography, High Pressure Liquid/standards , Female , Mass Spectrometry/methods , Mass Spectrometry/standards , Peptides, Cyclic/pharmacokinetics , Rats , Rats, Sprague-Dawley , Reproducibility of Results , Sensitivity and Specificity , Stereoisomerism
5.
Ciba Found Symp ; 158: 158-66; discussion 166-8, 1991.
Article in English | MEDLINE | ID: mdl-1718668

ABSTRACT

Dithioate DNA was synthesized and used for various biochemical studies. Results from these studies indicate that dithioate DNA is a potent inhibitor of HIV Reverse Transcriptase, activates endogenous RNase H in HeLa cell nuclear extracts, and is a useful probe for studying protein-DNA interactions.


Subject(s)
DNA/chemical synthesis , Thionucleotides/chemical synthesis , Base Sequence , DNA/metabolism , DNA/pharmacology , Enzyme Activation/drug effects , HIV/enzymology , Molecular Sequence Data , Reverse Transcriptase Inhibitors , Ribonuclease H/metabolism , Thionucleotides/metabolism , Thionucleotides/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL
...