Cic edizioni internazionali
Journal of Prenatal Medicine
Last issue of Journal of Prenatal Medicine

Journal of Prenatal Medicine

An International Journal of Prenatal Diagnosis and Fetal-Maternal Medicine

The JPM is the official journal of the Italian College of Fetal Maternal Medicine.

It introduces the newest and more interesting aspects of research in prenatal genetics, invasive procedures, ultrasound and high risk pregnancy.

The aim of the journal is to focus on the deep interactions among several aspects of genetic diagnostic, with a particular regard on molecular biology, ultrasound and biophysical diagnostic and studies on fetal diseases and anomalies. In general the scope is to publish the most interesting researches on pathophysiology, clinical and therapy in fetal-maternal-placental unit.
The journal prefers to publish easy editorial and mini-review articles in order to build the knowledge for introduce clinical guidelines. The articles will be carefully evaluated and selected to give absolutely corrected scientific contribute.

The journal is published quarterly and the articles will be reviewed by a scientific, dynamic committee.

Vol. 11 (No. 1-2) 2017 January-June

  1. Congenital cervical teratoma in association with neuronal migration disorder
    Saito-Benz M., Marlow J., Valsenti G., McKeown C., Baguley K., Berry M.J.
    doi: 10.11138/jpm/2017.11.1.001
  2. The cervical length correlates with the amount of bleeding during cesarean section of the pernicious placenta previa
    Yang S., Cao C., Li Q., Luo A., Ma L., Zeng W., Feng L.
    doi: 10.11138/jpm/2017.11.1.008
  3. Association between echogenic intracardiac focus in first trimester and biochemical screeningan analysis
    Kandasamy S., Raj S.P.
    doi: 10.11138/jpm/2017.11.1.014

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  1. Effect of vaginally administered DHA fatty acids on pregnancy outcome in high risk pregnancies for preterm delivery: a double blinded randomised controlled trial
    Giorlandino C., Brizzi C., Giorlandino M., Taramanni C., Mastrandrea M.L., Coco C., Mangiafico L., Cignini P., D'Emidio L., Raffio R., Padula F., Sebastianelli A., Nanni C., Carcioppolo O., Lena A., Giorgio E., Dugo N., Milite V., Lippa A., Vigna R., Giannarelli D., Mobili L.
    doi: 10.11138/jpm/2013.7.3.042
  2. Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosis
    Dello Russo C., Di Giacomo G., Mesoraca A., D'Emidio L., Iaconianni P., Minutolo E., Lippa A., Giorlandino C.
    doi: 10.11138/jpm/2014.8.1.017
  3. Prenatal diagnosis of giant cardiac rhabdomyoma with fetal hydrops in tuberous sclerosis
    Schlaegel F., Takacs Z., Solomayer E.F., Abdul-Kaliq H., Meyberg-Solomayer G.
    doi: 10.11138/jpm/2013.7.3.039
  4. Prenatal diagnosis of spinal muscular atrophy: clinical experience and molecular genetics of SMN gene analysis in 36 cases
    Derakhshan S.M., Abasalizadeh S., Abbasalizadeh F., Khaniani M.S.
    doi: 10.11138/jpm/2013.7.3.032
  5. Case report of prenatal diagnosis of Stüve-Wiedemann Syndrome in a woman with another child affected too
    Catavorello A., Vitale S.G., Rossetti D., Caldaci L., Panella M.M.
    doi: 10.11138/jpm/2013.7.3.035
  6. Predictive value of procalcitonin or c-reactive protein for subclinical intrauterine infection in patients with premature rupture of membranes (PROM)
    Li K., Yu H., Wang X., Liu X.
    doi: 10.11138/jpm/2016.10.3.023
  7. Fetal-MRI prenatal diagnosis of severe bilateral lung hypoplasia: alveolar capillary dysplasia case report
    Zirpoli S., Munari A.M., Rustico M., Bulfamante G., Lista G., Spaccini L., Cesaretti C.
    doi: 10.11138/jpm/2016.10.3.015
  8. Congenital cervical teratoma in association with neuronal migration disorder
    Saito-Benz M., Marlow J., Valsenti G., McKeown C., Baguley K., Berry M.J.
    doi: 10.11138/jpm/2017.11.1.001
  9. Introducing the next generation sequencing in genomic amnio and villuos sampling. The so called “Next Generation Prenatal Diagnosis” (NGPD)
    Giorlandino C., Mesoraca A., Bizzoco D., Dello Russo C., Cima A., Di Giacomo G., Cignini P., Padula F., Dugo N., D'Emidio L., Brizzi C., Raffio R., Milite V., Mangiafico L., Coco C., Carcioppolo O., Vigna R., Mastrandrea M., Mobili L.
    doi: 10.11138/jpm/2014.8.1.001
  10. A case of polimalformed fetus with a microdeletion of CTNNA3 gene
    Cancemi D., Urciuoli M., Morelli F., Lonardo M.C., Spampanato C., Ventruto M., Ventruto V., Sica C.
    doi: 10.11138/jpm/2016.10.3.020