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Orphanet Journal of Rare Diseases
|
March 11, 2025
Pregnancy-related issues in rare and low-prevalence diseases: results of ERN transversal working group on pregnancy and family planning survey
Dina Zucchi, Diana Marinello, Chiara Tani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 23, 2020
Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation
Solveig Heide, Myrtille Spentchian, Stéphanie Valence, et al.
Reproductive Health
|
November 26, 2025
Addressing unmet needs in pregnancy and family planning of people living with rare and low-prevalence diseases: results of the "ERN transversal working group on pregnancy and family planning" survey
Giovanni Fulvio, Diana Marinello, Dina Zucchi, et al.
Kidney International
|
August 5, 2020
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease
Julie Klein, Bénédicte Buffin-Meyer, Franck Boizard, et al.
Journal of Medical Genetics
|
April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Annales De Biologie Clinique
|
August 15, 2014
[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement]
Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement
|
November 8, 2016
French law: what about a reasoned reimbursement of serum vitamin D assays?
Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Page
of 33
Search research articles
Search
Showing results (321-330 of 327) with videos related to
Sort By:
Page
of 33
You have reached the last page of results.
This site can display upto 327 results.
Orphanet Journal of Rare Diseases
|
March 11, 2025
Pregnancy-related issues in rare and low-prevalence diseases: results of ERN transversal working group on pregnancy and family planning survey
Dina Zucchi, Diana Marinello, Chiara Tani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 23, 2020
Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation
Solveig Heide, Myrtille Spentchian, Stéphanie Valence, et al.
Reproductive Health
|
November 26, 2025
Addressing unmet needs in pregnancy and family planning of people living with rare and low-prevalence diseases: results of the "ERN transversal working group on pregnancy and family planning" survey
Giovanni Fulvio, Diana Marinello, Dina Zucchi, et al.
Kidney International
|
August 5, 2020
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease
Julie Klein, Bénédicte Buffin-Meyer, Franck Boizard, et al.
Journal of Medical Genetics
|
April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Annales De Biologie Clinique
|
August 15, 2014
[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement]
Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement
|
November 8, 2016
French law: what about a reasoned reimbursement of serum vitamin D assays?
Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Page
of 33