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Erratum to: The effect of dabigatran and rivaroxaban on platelet reactivity and inflammatory markers.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
The effect of dabigatran and rivaroxaban on platelet reactivity and inflammatory markers.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2015, v. 40, n. 3, p. 340, doi. 10.1007/s11239-015-1245-z
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- Publication type:
- Article
Relation between ticagrelor response and levels of circulating reticulated platelets in patients with non-ST elevation acute coronary syndromes.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2015, v. 40, n. 2, p. 211, doi. 10.1007/s11239-015-1178-6
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- Publication type:
- Article
Circulating reticulated platelets over time in patients with myocardial infarction treated with prasugrel or ticagrelor.
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- Journal of Thrombosis & Thrombolysis, 2015, v. 40, n. 1, p. 70, doi. 10.1007/s11239-014-1156-4
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- Publication type:
- Article
Exposure to platelets promotes functional properties of endothelial progenitor cells.
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- Journal of Thrombosis & Thrombolysis, 2010, v. 30, n. 4, p. 398, doi. 10.1007/s11239-010-0514-0
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- Publication type:
- Article
Effect of vitamin D on endothelial progenitor cells function.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0178057
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- Publication type:
- Article
White matter abnormalities and iron deposition in prenatal mucolipidosis IV- fetal imaging and pathology.
- Published in:
- Metabolic Brain Disease, 2021, v. 36, n. 7, p. 2155, doi. 10.1007/s11011-021-00742-3
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- Publication type:
- Article
Metabolic stroke in a patient with bi-allelic OPA1 mutations.
- Published in:
- Metabolic Brain Disease, 2019, v. 34, n. 4, p. 1043, doi. 10.1007/s11011-019-00415-2
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- Publication type:
- Article
Agenesis of the corpus callosum. An autopsy study in fetuses.
- Published in:
- 2016
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- Publication type:
- journal article
Autosomal Dominant, Long-Standing Dysglycemia in 2 Families with Unique Phenotypic Features.
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- Clinical Medicine Insights: Endocrinology & Diabetes, 2024, p. 1, doi. 10.1177/11795514241259740
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- Publication type:
- Article
Periventricular pseudocysts of noninfectious origin: Prenatal associated findings and prognostic factors.
- Published in:
- 2020
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- Publication type:
- journal article
Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?
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- Prenatal Diagnosis, 2011, v. 31, n. 4, p. 360, doi. 10.1002/pd.2694
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- Publication type:
- Article
The fetal cerebellum. Pitfalls in diagnosis and management.
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- Prenatal Diagnosis, 2009, v. 29, n. 4, p. 372, doi. 10.1002/pd.2196
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- Publication type:
- Article
Familial occurrence of isolated nonseptated nuchal cystic hygromata in midtrimester of pregnancy.
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- Prenatal Diagnosis, 2004, v. 24, n. 4, p. 260, doi. 10.1002/pd.849
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- Publication type:
- Article
Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNA.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 1, p. 31, doi. 10.1002/pd.516
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- Publication type:
- Article
Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33A.
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- Human Mutation, 2022, v. 43, n. 12, p. 2265, doi. 10.1002/humu.24479
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- Publication type:
- Article
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 6, p. 623, doi. 10.1002/acn3.198
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- Publication type:
- Article
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletions.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 3, p. 287, doi. 10.1038/ejhg.2010.213
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- Publication type:
- Article
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 226, doi. 10.1038/sj.ejhg.5200791
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- Publication type:
- Article
De novo hotspot variants in CYFIP2 cause early-onset epileptic encephalopathy.
- Published in:
- 2018
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- Publication type:
- journal article
Mutations of the thyroid hormone transporter MCT8 cause prenatal brain damage and persistent hypomyelination.
- Published in:
- 2014
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- Publication type:
- journal article
Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders.
- Published in:
- Reproductive Biology & Endocrinology, 2003, v. 1, p. 110, doi. 10.1186/1477-7827-1-110
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- Publication type:
- Article
The Effect of Tafamidis on Circulating Endothelial Progenitor Cells in Patients with Transthyretin Cardiac Amyloidosis.
- Published in:
- Cardiovascular Drugs & Therapy, 2022, v. 36, n. 3, p. 489, doi. 10.1007/s10557-021-07265-0
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- Publication type:
- Article
Impact of Calcium Channel Blockers on Aspirin Reactivity in Patients with Coronary Artery Disease.
- Published in:
- Cardiovascular Drugs & Therapy, 2022, v. 36, n. 3, p. 467, doi. 10.1007/s10557-021-07295-8
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- Publication type:
- Article
The Effect of Proprotein Convertase Subtilisin Kexin Type 9 Inhibitors on Circulating Endothelial Progenitor Cells in Patients with Cardiovascular Disease.
- Published in:
- Cardiovascular Drugs & Therapy, 2022, v. 36, n. 1, p. 85, doi. 10.1007/s10557-020-07119-1
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- Publication type:
- Article
Diagnosis of fetal cortical abnormalities by new reference charts for assessment of sylvian fissure biometry.
- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 8, p. 1066, doi. 10.1002/pd.6359
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- Publication type:
- Article
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation.
- Published in:
- Acta Neuropathologica, 2012, v. 124, n. 4, p. 575, doi. 10.1007/s00401-012-1007-3
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- Publication type:
- Article
Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRI.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Familial Brain Periventricular Pseudocysts.
- Published in:
- 2017
- By:
- Publication type:
- journal article
The 'Brain Shadowing Sign': A Novel Marker of Fetal Craniosynostosis.
- Published in:
- 2016
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- Publication type:
- journal article
Hemifacial Microsomia with Spinal and Rib Anomalies: Prenatal Diagnosis and Postmortem Confirmation Using 3-D Computed Tomography Reconstruction.
- Published in:
- Fetal Diagnosis & Therapy, 2011, v. 30, n. 4, p. 309, doi. 10.1159/000330121
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- Publication type:
- Article
Imaging of Fetal Cytomegalovirus Infection.
- Published in:
- Fetal Diagnosis & Therapy, 2011, v. 29, n. 2, p. 117, doi. 10.1159/000321346
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- Publication type:
- Article
Imaging of fetal cytomegalovirus infection.
- Published in:
- 2011
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- Publication type:
- journal article
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome.
- Published in:
- 2003
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- Publication type:
- journal article
Elevated galectin-3 in women with gestational diabetes mellitus, a new surrogate for cardiovascular disease in women.
- Published in:
- PLoS ONE, 2020, v. 15, n. 6, p. 1, doi. 10.1371/journal.pone.0234732
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- Publication type:
- Article
Small size, big problems: insights and difficulties in prenatal diagnosis of fetal microcephaly.
- Published in:
- Frontiers in Neuroscience, 2024, p. 01, doi. 10.3389/fnins.2024.1347506
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- Publication type:
- Article
Thrombogenicity and endothelial progenitor cells function during Acute myocardial infarction - comparison of Prasugrel versus Ticagrelor.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2023, v. 55, n. 3, p. 407, doi. 10.1007/s11239-022-02759-6
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- Publication type:
- Article
The effect of cessation of 2nd generation P<sub>2</sub>Y<sub>12</sub> inhibitor therapy on platelet reactivity in patients 1 year after acute myocardial infarction.
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- Journal of Thrombosis & Thrombolysis, 2018, v. 46, n. 3, p. 351, doi. 10.1007/s11239-018-1701-7
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- Publication type:
- Article
Characterization of surface antigens of reticulated immature platelets.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2017, v. 44, n. 3, p. 291, doi. 10.1007/s11239-017-1533-x
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- Publication type:
- Article
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families.
- Published in:
- Genome Biology, 2011, v. 12, n. 9, p. 2, doi. 10.1186/gb-2011-12-9-r89
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- Publication type:
- Article
Expanding the natural history of CASK‐related disorders to the prenatal period.
- Published in:
- Developmental Medicine & Child Neurology, 2023, v. 65, n. 4, p. 544, doi. 10.1111/dmcn.15419
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- Publication type:
- Article
Unilateral Gynecomastia in an Adolescent with Poland Syndrome: A Clue for Diagnosis.
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- Israel Medical Association Journal, 2023, v. 25, n. 7, p. 505
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- Publication type:
- Article
The Effect of Mineralocorticoid Receptor Antagonists on Recruitment and Function of Endothelial Progenitor Cells in Patients with Congestive Heart Failure.
- Published in:
- Israel Medical Association Journal, 2018, v. 20, n. 4, p. 233
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- Publication type:
- Article
Microarray findings in pregnancies with oligohydramnios – a retrospective cohort study and literature review.
- Published in:
- Journal of Perinatal Medicine, 2020, v. 48, n. 1, p. 53, doi. 10.1515/jpm-2019-0228
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- Publication type:
- Article
Reticulated Platelets and Their Relationship with Endothelial Progenitor Cells during the Acute Phase of ST-Elevation Myocardial Infarction.
- Published in:
- Journal of Clinical Medicine, 2022, v. 11, n. 21, p. 6597, doi. 10.3390/jcm11216597
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- Publication type:
- Article
Pathways Mediating the Interaction between Endothelial Progenitor Cells (EPCs) and Platelets.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0095156
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- Publication type:
- Article
The Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Gene VRK1 Regulates Neuronal Migration through an Amyloid-β Precursor Protein-Dependent Mechanism.
- Published in:
- Journal of Neuroscience, 2015, v. 35, n. 3, p. 936, doi. 10.1523/JNEUROSCI.1998-14.2015
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- Publication type:
- Article
Successful pregnancy in a patient with mitochondrial cardiomyopathy due to ACAD9 deficiency.
- Published in:
- Journal of Inherited Metabolic Disease Reports, 2020, v. 56, n. 1, p. 9, doi. 10.1002/jmd2.12157
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- Publication type:
- Article
In-silico phenotype prediction by normal mode variant analysis in TUBB4A-related disease.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04337-x
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- Publication type:
- Article
Generation of vascular chimerism within donor organs.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-92823-7
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- Publication type:
- Article