ABD e-News, May 23, 2003

Newsletter for State of Iowa Alcoholic Beverages Division

Relació entre el percentatge i número absolut de cèl·lules Natural Killer i de l’expressió dels seus receptors NKG2D i NKp46 i les diferents formes de presentació de la Tuberculosi. Resultats preliminars.

La tuberculosi pot localitzar-se al pulmó: TB-P o altres òrgans: TB-EP, segons el compromís del sistema immunitari de l’hoste, on hi intervenen les cèl.lules Natural Killer-NK. L’estudi analitza el percentatge i número absolut d’NK i l’expressió dels receptors d’activació, NKG2D - NKp46, en 15 malalts/TB-P, 15 malalts/TB-EP i 15 sans, trobant-se augmentades en percentatge en el grup TB-P, disminuïdes en número absolut en els TB-EP i TB-P, i valors més alts d’ NKG2D, sobretot, malalts de TB-EP. Les coincidències amb d’altres estudis i les troballes preliminars obren possibilitats a investigacions en el camp de la TB-EP i la reacció immune.

Lottery Action, September 23-October 6, 2002, Vol. 9, no. 18

Newsletter for Iowa Lottery

Lottery Action, December 2-15 2002, Vol. 9, no. 23

Newsletter for Iowa Lottery

Lottery Action, February 10-23 2003, Vol.10, no.3

Newsletter for Iowa Lottery

Missing Persons Summary, June 23, 2003

Missing persons summary

Lottery Action, November 17-30, 2003, Vol. 10, no. 23

Newsletter for Iowa Lottery

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.

Interstitial deletions of 7q11.23 cause Williams-Beuren syndrome, one of the best characterized microdeletion syndromes. The clinical phenotype associated with the reciprocal duplication however is not well defined, though speech delay is often mentioned. We present 14 new 7q11.23 patients with the reciprocal duplication of the Williams-Beuren syndrome critical region, nine familial and five de novo. These were identified by either array-based MLPA or by array-CGH/oligonucleotide analysis in a series of patients with idiopathic mental retardation with an estimated population frequency of 1:13,000-1:20,000. Variable speech delay is a constant finding in our patient group, confirming previous reports. Cognitive abilities range from normal to moderate mental retardation. The association with autism is present in five patients and in one father who also carries the duplication. There is an increased incidence of hypotonia and congenital anomalies: heart defects (PDA), diaphragmatic hernia, cryptorchidism and non-specific brain abnormalities on MRI. Specific dysmorphic features were noted in our patients, including a short philtrum, thin lips and straight eyebrows. Our patient collection demonstrates that the 7q11.23 microduplication not only causes language delay, but is also associated with congenital anomalies and a recognizable face.

Arrêt du Conseil d'Etat du Roi, qui ordonne la réunion de l'imprimerie du Cabinet à l'Imprimerie royale du Louvre et l'établissement d'un détachement de ladite Imprimerie royale à Versailles. Du 23 mai 1789...

[Acte. 1789-03-23]

ABD e-News, January 23, 2004

Weekly newsletter for the State of Iowa Alcoholic Beverages Division

Laurentz, Mme Golding, Decugis, Mme Beamish, 23-11-19, clubiste de tennis : [photographie de presse] / [Agence Rol]

Référence bibliographique : Rol, 57030