Check the papers we recently published and helped publish

Our team has more than 15 years of experience in scientific and medical research and we have been helping researchers publish their papers for more than 3 years.

Check below some of the papers we worked on:

2012

Hyperbilirubinemia and Neurodevelopmental Outcome of Very Low Birthweight Infants: Results from the LIFT Cohort.
PLoS One. 2012;7:e30900. PMID: 22303470

Epidemiology of Dandruff, Scalp Pruritus and Associated Symptoms.
Acta Derm Venereol. 2012 Jan 26. PMID: 22277979

Predictors of poor blood pressure control assessed by 24 hour monitoring in patients with type B acute aortic dissection.
Vasc Health Risk Manag. 2012;8:23-30. PMID: 22272072

CT image quality improvement using adaptive iterative dose reduction with wide-volume acquisition on 320-detector CT.
Eur Radiol. 2012;22:295-301. PMID: 21927791

The gender gap in stroke: a meta-analysis.
Acta Neurol Scand. 2012;125:83-90. PMID: 21649609

2011

Renal cell carcinoma with MiTF/TFE3 translocation in children: Report of a case at the stage of lymph node involvement.
Afr J Paediatr Surg. 2011;8:317-9. PMID: 22248899

An example of extreme cardiology: chest pain on the high seas and helicoptered medical evacuations The French Navy experience.
Am J Emerg Med. 2011 Dec 26. PMID: 22205005

Practical questions around individual with a pacemaker or an implantable cardioverter defibrillator.
Presse Med. 2011 Dec 2. PMID: 22138293

Not all sarcomas developed in irradiated tissue are necessarily radiation-induced – Spectrum of disease and treatment characteristics.
Crit Rev Oncol Hematol. 2011 Dec 2. PMID: 22138059

A French hospital sentenced for unreasonable obstinacy.
Eur J Health Law. 2011;18:521-30. PMID: 22128520

MMP-2/MMP-9 plasma level and brain expression in cerebral amyloid angiopathy-associated hemorrhagic stroke.
Brain Pathol. 2011 Jun 27. PMID: 21707819

Etiology and current clinical characteristics of male urethral stricture disease: experience from a public teaching hospital in Senegal.
Urol Nephrol. 2011;43:969-74. PMID: 21442395

Drug-induced lichenoid reaction after kyphoplasty.
Allergy. 2011;66:1494-5. PMID: 21645013

Screening for prostate cancer by digital rectal examination and PSA determination in Senegal.
ISRN Oncol. 2011;2011:943704. PMID: 22091437

Update on the serum biomarkers and genetic factors associated with safety and efficacy of rt-PA treatment in acute stroke patients.
Stroke Res Treat. 2011;2011:182783. PMID: 21772966

Acute leukoencephalopathy after buprenorphine intoxication in a 2-year-old child.
Eur J Paediatr Neurol. 2011;15:368-71. PMID: 21450498

Causes of mortality associated with HIV/AIDS in health-care facilities in Togo: a six-month prospective study.
Trop Doct. 2011;41:215-217. PMID: 21914672

No evidence of APP point mutation and locus duplication in individuals with cerebral amyloid angiopathy.
Eur J Neurol. 2011;18:1279-81. PMID: 21463452

A large screening of angiogenesis biomarkers and their association with neurological outcome after ischemic stroke.
Atherosclerosis. 2011;216:205-11. PMID: 21324462

Brain perihematoma genomic profile following spontaneous human intracerebral hemorrhage.
PLoS One. 2011;6:e16750. PMID: 21311749

Leukoaraiosis is associated with genes regulating blood-brain barrier homeostasis in ischaemic stroke patients.
Eur J Neurol. 2011;18:826-35. PMID: 21122033

Osteopontin predicts long-term functional outcome among ischemic stroke patients.
J Neurol. 2011;258:486-93. PMID: 20967551

ACE variants and risk of intracerebral hemorrhage recurrence in amyloid angiopathy.
Neurobiol Aging. 2011;32:551.e13-22. PMID: 20381197

2010

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL. (1)
Hum Genet. 2010;127:474. PMID: 21488300

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL. (2)
Hum Genet. 2010;127:473-4. PMID: 21488283

A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population.
Neurology. 2010;75:2033-5. PMID: 21115960

CD40-1C>T polymorphism (rs1883832) is associated with brain vessel reocclusion after fibrinolysis in ischemic stroke.
Pharmacogenomics. 2010 Jun;11(6):763-72. PMID: 20504251

The I/D polymorphism of the ACE1 gene is not associated with ischaemic stroke in Spanish individuals.
Eur J Neurol. 2010;17:1390-2. PMID: 20402757

PAI-1 4G/5G polymorphism is associated with brain vessel reocclusion after successful fibrinolytic therapy in ischemic stroke patients.
Int J Neurosci. 2010;120:245-251. PMID: 20374070

Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke: a case-control, meta-analysis and functional study.
Cerebrovasc Dis. 2010;29:528-537. PMID: 20357438

KCNK17 genetic variants in ischemic stroke.
Atherosclerosis. 2010;208:203-209. PMID: 19647252

2009

CADASIL management or what to do when there is little one can do.
Expert Rev Neurother. 2009;9:197-210. PMID: 19210195

2008

Genetics of stroke: a review of recent advances.
Expert Rev Mol Diagn. 2008;8:495-513. PMID: 18598230

Association between ESR2 genetic variants and risk of myocardial infarction.
Clin Chem. 2008;54:1183-1189. PMID: 18487282

2006

Relationship of classical and non-classical risk factors with genetic variants relevant to coronary heart disease.
Eur J Cardiovasc Prev Rehabil. 2006;13:738-744. PMID: 17001213

 
 

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