Search results for "BN"

Uterus Transplantation

2018

Uterus transplantation (UTx) has been successfully introduced as a treatment option for women with absolute uterine factor infertility (AUFI). AUFI representing approximately 3% to 5% of the female general population is linked to either congenital uterine agenesis (Mayer-Rokitansky-Küster-Hauser syndrome), major congenital uterine malformation (hypoplastic uterus, fraction of bicornuate/unicornuate uterus), a surgically absent uterus, or an acquired condition (intrauterine adhesions, leiomyoma) linked to uterine malfunction that causes implantation failure or defect placentation. The world's first clinical uterus transplant was performed in 2000. However, a hysterectomy became necessary sho…

Limits on neutral Higgs boson production in the forward region in $pp$ collisions at $\sqrt{s} = 7$ TeV

2013

Limits on the cross-section times branching fraction for neutral Higgs bosons, produced in p p collisions at root s = 7 TeV, and decaying to two tau leptons with pseudorapidities between 2.0 and 4.5, are presented. The result is based on a dataset, corresponding to an integrated luminosity of 1.0 fb(-1), collected with the LHCb detector. Candidates are identified by reconstructing final states with two muons, a muon and an electron, a muon and a hadron, or an electron and a hadron. A model independent upper limit at the 95% confidence level is set on a neutral Higgs boson cross-section times branching fraction. It varies from 8.6 pb for a Higgs boson mass of 90 GeV to 0.7 pb for a Higgs bos…

Sperm Telomere Length in Men with Normal and Abnormal semen Parameters. A Pilot Study

2019

Objective: Male infertility is a growing social problem. The measurement of telomere length may be a new marker that can help to assess reproductive age of males and assess the chances of in vitro fertilization. Aim: The aim of our study was to investigate whether there are any differences between telomere length in men with normal and abnormal semen parameters. Materials and Methods: Telomere length was analyzed in 17 patients with normal and 28 patients with abnormal semen parameters using the telomeric repeat amplification protocol and Quantitative Real-Time Polymerase Chain Reaction (qPCR). Results: Mean sperm telomere length in all donors was 49±24kbp per haploid genome. However, patie…

Observatoire francophone des néoplasies endocriniennes multiples de type 1. Un outil du Groupe d'étude des Tumeurs Endocrines (GTE)

2007

Wermer's syndrome or Multiple Endocrine Neoplasia Type-1 (MEN1) is an autosomal dominant inherited disease, related to mutations in MEN1, an approximately 10-kb gene encoding menin, localized on chromosome 11q13. The Endocrine Tumor Group (GTE) has set up a MEN1 observatory of 1001 regularly followed MEN1 cases. This observatory aims at registering and evaluating MEN1 cases in a large cohort. Any new study on a particular unexplored aspect of the disease may be proposed by a physician to the GTE. This article describes the way to diagnose a new MEN1 case and to register it. Procedures for participating in a new study are presented. Some original results are quoted.

Dydrogesterone use during pregnancy: Overview of birth defects reported since 1977

2009

Between 1977 and 2005, 28 cases of potential links between maternal dydrogesterone use during pregnancy and congenital birth defects were reported. The types of defects were very diverse, with no evidence of a pattern of abnormalities. The data do not provide evidence for congenital malformations associated with dydrogesterone use.

Prä- und postnatales Nierenscreening im Vergleich: eine Analyse von 34.450 Neugeborenen des Geburtenregisters Mainzer Modell

2002

Zielsetzung. Fehlbildungen des internen Urogenitalsystems sind haufig und stellen die zweithaufigste Organkategorie dar. Anhand des Mainzer Geburtenregisters werden populationsbezogene Pravalenzen von Nierenfehlbildungen, die Sensitivitat des pranatalen Ultraschalls und die Haufigkeit operationsbedurftiger Befunde ermittelt. Material und Methode. Im Zeitraum von 1990–2001 erhielten alle in Mainz geborenen Kinder neben einer klinischen Untersuchung eine Ultraschalluntersuchung der ableitenden Harnwege. Bei Totgeborenen, Spontanaborten (≥15. SSW) und induzierten Aborten wurden die Befunde der Pathologie in die Erfassung einbezogen. Seit 1996 (nach Einfuhrung des Fehlbildungsschalles in die Mu…

Kraniometrische Merkmale bei unterschiedlichen Anomalien

1972

Die vorangegangenen Ausfuhrungen verfolgten das Ziel, die Frage aufzuhellen, ob fur Anomalien des Kieferbereiches eine weitgehende Unabhangigkeit vom Aufbau des Gesichtsschadels besteht. Zu diesem Zweck wurden je 10 Fernrontgen-Profilaufnahmen von 5 typischen Anomaliegruppen ausgewahlt und im Hinblick auf die Fragestellung ausgewertet. Das mit Hilfe biostatistischer Verfahren gewonnene Ergebnis gibt zu erkennen, das keine der gewahlten Variablen des Gesichtsschadels eine spezifische Zuordnung zu einer bestimmten Anomaliegruppe ermoglichte. Zwischen kraniometrischen Merkmalen und Gebisanomalien bestehen demnach keine engeren Beziehungen.

REMARKS ON THE HIGGS-PARTICLE PREDICTION IN THE STANDARD MODEL

2003

Precision measurement of D meson mass differences

2013

Using three- and four-body decays of D mesons produced in semileptonic b-hadron decays, precision measurements of D meson mass differences are made together with a measurement of the D-0 mass. The measurements are based on a dataset corresponding to an integrated luminosity of 1.0 fb(-1) collected in pp collisions at 7 TeV. Using the decay D-0 -> K+K-K-pi(+), the D-0 mass is measured to be M(D-0) = 1864.75 +/- 0.15 (stat) +/- 0.11 (syst) MeV/c(2). The mass differences M(D+) - M(D-0) = 4.76 +/- 0.12 (stat) +/- 0.07 (syst) MeV/c(2), M(D-s(+)) - M(D+) = 98.68 +/- 0.03 (stat) +/- 0.04 (syst) MeV/c(2) are measured using the D-0 -> K+K-pi(+)pi(-) and D-(s)(+) -> K+K-pi(+) modes.

Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of zellweger: Comparative pathology

1976

A study of 11 autopsied cases of the cerebro-hepato-renal syndrome of Zellweger (ZS) is reported. All cases had severe, persistent congenital hypotonia, hepatic lobular disarray, renal cortical cysts and pulmonary hypoplasia. Many had cardiovascular malformations, hepatomegaly, cerebral cortical gyral maldevelopment and pancreatic islet hyperplasia. Additional, less frequent findings are delineated. Results of iron content studies of hepatic and renal tissues are related to age of survival and possible development of fibrosis.