Rainer Bald

Leverkusen, NW, Germany

Last Updated: 09/26/2026

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Found 12 publications

Intrauterine transfusion in 103 fetuses with severe anemia caused by parvovirus infection. A multicenter retrospective study.

Intrauterine transfusion in 103 fetuses with severe anemia caused by parvovirus infection. A multicenter retrospective study.

Journal: Archives of gynecology and obstetrics

Published: May 19, 2022

Updated DEGUM Quality Requirements for the Basic Prenatal Screening Ultrasound Examination (DEGUM Level I) between 18 + 0 and 21 + 6 weeks of gestation.

Updated DEGUM Quality Requirements for the Basic Prenatal Screening Ultrasound Examination (DEGUM Level I) between 18 + 0 and 21 + 6 weeks of gestation.

Journal: Ultraschall in der Medizin (Stuttgart, Germany : 1980)

Published: January 04, 2020

Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.

Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.

Journal: Birth defects research

Published: August 23, 2019

Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.

Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.

Journal: American journal of medical genetics. Part A

Published: November 16, 2017

D blocking phenomenon overcome.

D blocking phenomenon overcome.

Journal: Transfusion

Published: July 06, 2017

Fetal Pathology of Neural Tube Defects - An Overview of 68 Cases.

Fetal Pathology of Neural Tube Defects - An Overview of 68 Cases.

Journal: Geburtshilfe und Frauenheilkunde

Published: December 03, 2016

Early Intrauterine Transfusion in Fetuses with Severe Anemia Caused by Parvovirus B19 Infection.

Early Intrauterine Transfusion in Fetuses with Severe Anemia Caused by Parvovirus B19 Infection.

Journal: Fetal diagnosis and therapy

Published: October 21, 2016

Prenatal diagnosis of congenital cytomegalovirus infection in 115 cases: a 5 years' single center experience.

Prenatal diagnosis of congenital cytomegalovirus infection in 115 cases: a 5 years' single center experience.

Journal: Prenatal diagnosis

Published: September 19, 2016

Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus.

Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus.

Journal: American journal of medical genetics. Part A

Published: September 07, 2016

Successful treatment of an infant with CDA type II by intrauterine transfusions and postnatal stem cell transplantation.

Successful treatment of an infant with CDA type II by intrauterine transfusions and postnatal stem cell transplantation.

Journal: Pediatric blood & cancer

Published: May 15, 2013

Serological and virological analysis of maternal and fetal blood samples in prenatal human parvovirus b19 infection.

Serological and virological analysis of maternal and fetal blood samples in prenatal human parvovirus b19 infection.

Journal: The Journal of infectious diseases

Published: January 26, 2012

Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly.

Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly.

Journal: European journal of human genetics : EJHG

Published: January 20, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026