Nicole Meyer

[The use of medical services and the utilization rate in screening programs in relation to social class: results of a representative survey in Bavaria].

Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences.

C. elegans PAR proteins function by mobilizing and stabilizing asymmetrically localized protein complexes.

The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development.

Four and one-half-year follow-up of the effectiveness of diphtheria-tetanus toxoids-acellular pertussis/Haemophilus influenzae type b and diphtheria-tetanus toxoids-acellular pertussis-inactivated poliovirus/H. influenzae type b combination vaccines in Germany.

Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data.

Personal dosimetry of exposure to mobile telephone base stations? An epidemiologic feasibility study comparing the Maschek dosimeter prototype and the Antennessa SP-090 system.

A novel DFNA5 mutation does not cause hearing loss in an Iranian family.

Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.

Sonographic measurement of the lower uterine segment thickness: is it truly predictive of uterine rupture?

Genetic analysis of the Caenorhabditis elegans GLH family of P-granule proteins.

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.

Human male infertility caused by mutations in the CATSPER1 channel protein.

Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.

[Validity of the axis "conflicts" of the Operationalized Psychodynamic Diagnostics (OPD)].

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population.

[Quality characteristics concerning pain therapy].

Genetic male infertility and mutation of CATSPER ion channels.

A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome.

Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.

Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.

The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.

Knowledge levels of pharmaceutical sales representatives in pain therapy: a descriptive questionnaire-based study.

Rotavirus shedding in premature infants following first immunization.

Paramedics experiences and expectations concerning advance directives: a prospective, questionnaire-based, bi-centre study.

Causes of alternative pathway dysregulation in dense deposit disease.

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.

A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran.

Impact of chemotherapeutic agents on the immunostimulatory properties of human 6-sulfo LacNAc+ (slan) dendritic cells.

Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.

A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome.

Soluble CR1 therapy improves complement regulation in C3 glomerulopathy.

Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome.

Pharmacokinetic and pharmacodynamic effects of methylphenidate and MDMA administered alone or in combination.

Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.

Topiramate use in pregnancy and the birth prevalence of oral clefts.

TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss.

A new microfluidics-based droplet dispenser for ICPMS.

Healthcare Resource Use and Expenditures among Metastatic Breast Cancer Patients Treated with HER2-Targeted Agents.

Retrospective database analysis of clinical outcomes and costs for treatment of abnormal uterine bleeding among women enrolled in US Medicaid programs.

Defining the complement biomarker profile of C3 glomerulopathy.

Treatment patterns and survival in metastatic breast cancer patients by tumor characteristics.

Comparison of direct and indirect costs of abnormal uterine bleeding treatment with global endometrial ablation and hysterectomy.

Economic burden associated with adverse events in patients with metastatic melanoma.

Heme oxygenase-1 is critically involved in placentation, spiral artery remodeling, and blood pressure regulation during murine pregnancy.

Transfer of regulatory T cells into abortion-prone mice promotes the expansion of uterine mast cells and normalizes early pregnancy angiogenesis.

Chymase-producing cells of the innate immune system are required for decidual vascular remodeling and fetal growth.

Safeguarding of Fetal Growth by Mast Cells and Natural Killer Cells: Deficiency of One Is Counterbalanced by the Other.

Simultaneous Ablation of Uterine Natural Killer Cells and Uterine Mast Cells in Mice Leads to Poor Vascularization and Abnormal Doppler Measurements That Compromise Fetal Well-being.

Bisphenol A exposure during early pregnancy impairs uterine spiral artery remodeling and provokes intrauterine growth restriction in mice.

Mast cells-Good guys with a bad image?