Publications by authors named "Ieva Grinfelde"

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Altered Splicing of in a Multigenerational Family from Latvia Affected by Danon Disease.
Janis Stavusis, Ieva Micule, Ieva Grinfelde, Anna Zdanovica, Janis Pudulis

Medicina (Kaunas)· January 2024

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Treatment of latent tuberculosis in a child with mucopolysaccharidosis type I receiving enzyme replacement therapy: A case report.
Lauma Vasilevska, Madara Auzenbaha, Ieva Grinfelde, Anita Skangale

Front Pediatr· August 2022

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Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology.
Ferdinand Dhombres, Patricia Morgan, Bimal P Chaudhari, Isabel Filges, Teresa N Sparks, Ieva Grinfelde

Am J Med Genet C Semin Med Genet· June 2022

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Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia.
Baiba Lace, Ieva Micule, Viktorija Kenina, Signe Setlere, Jurgis Strautmanis, Ieva Grinfelde

Neurol Genet· June 2022

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Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6).
Marija Jurčenko, Madara Auzenbaha, Ieva Mičule, Ieva Grīnfelde, Aigars Dzalbs

Am J Case Rep· February 2022

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Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study.
Baiba Lace, Sander Pajusalu, Diana Livcane, Ieva Grinfelde, Ilze Akota

Front Genet· February 2022

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A novel variant causing X-linked hypohidrotic ectodermal dysplasia: Case report.
Baiba Alksere, Liene Kornejeva, Ieva Grinfelde, Aigars Dzalbs, Dace Enkure

Mol Genet Metab Rep· December 2021

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Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia.
Arta Katkevica, Madara Kreile, Ieva Grinfelde, Gita Taurina, Ieva Micule

Case Rep Med· November 2021

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The outcomes after transfers of embryos with chromosomal mosaicism: a single reproductive medicine center experience at iVF Riga clinic.
Baiba Alksere, Ieva Grinfelde, Liene Kornejeva, Aigars Dzalbs, Natalija Vedmedovska

Gynecol Endocrinol· October 2021

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Case of Inherited Partial AZFa Deletion without Impact on Male Fertility.
Baiba Alksere, Dace Berzina, Alesja Dudorova, Una Conka, Santa Andersone, Ieva Grinfelde

Case Rep Genet· October 2019

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Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe.
Ingeborg Barisic, Ljubica Boban, Diana Akhmedzhanova, Jorieke E H Bergman, Clara Cavero-Carbonell, Ieva Grinfelde

Eur J Med Genet· September 2018

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BCL3 gene role in facial morphology.
Baiba Lace, Inga Kempa, Janis Klovins, Janis Stavusis, Astrida Krumina, Ieva Grinfelde

Birth Defects Res A Clin Mol Teratol· November 2012

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Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin.
Baiba Lace, Inga Kempa, Linda Piekuse, Ieva Grinfelde, Janis Klovins

Eur J Oral Sci· December 2011

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