Found: 31
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The impact of RAS mutation on the treatment strategy of colorectal cancer.
- Published in:
- Medicine & Pharmacy Reports: Clujul Medical, 2023, v. 96, n. 1, p. 5, doi. 10.15386/mpr-2408
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- Article
Explorarea deficitelor intelectuale în distrofia musculară Duchenne și Becker.
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- Journal for Neurology & Psychiatry of Child & Adolescent in Romania, 2024, v. 30, n. 3, p. 15
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- Article
Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array.
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- Journal of Personalized Medicine, 2024, v. 14, n. 3, p. 290, doi. 10.3390/jpm14030290
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- Article
Respiratory pathology in a patient with muscular dystrophy.
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- Pneumologia, 2022, v. 71, n. 2, p. 81, doi. 10.2478/pneum-2023-0025
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- Article
Changes in skeletal dysplasia nosology.
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- Romanian Journal of Morphology & Embryology, 2021, v. 62, n. 3, p. 689, doi. 10.47162/RJME.62.3.05
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- Article
Cardiofaciocutaneous syndrome - a longitudinal study of a case over 33 years: case report and review of the literature.
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- Romanian Journal of Morphology & Embryology, 2021, v. 62, n. 2, p. 563, doi. 10.47162/RJME.62.2.23
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- Article
Cherubism: a case report.
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- Romanian Journal of Morphology & Embryology, 2014, v. 55, p. 655
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- Article
Treatment Strategies' Impact on Progression-Free Survival According to RMST Function in Metastatic Colorectal Cancer Patients: A Retrospective Study from Romania.
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- Journal of Clinical Medicine, 2024, v. 13, n. 20, p. 6174, doi. 10.3390/jcm13206174
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- Article
Prenatal Diagnosis and Genetic Counselling in Turner Syndrome: Case Report and Literature Review.
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- Medicina Moderna, 2018, v. 25, n. 3, p. 107
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- Article
Recognition of early warning signs and symptoms - the first steps on the road to Autism Spectrum Disorder diagnosis.
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- Annali dell'Istituto Superiore di Sanita, 2022, v. 58, n. 3, p. 183, doi. 10.4415/ANN_22_03_07
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- Article
Health systems sustainability in the framework of rare diseases actions. Actions on educational programmes and training for professionals and patients.
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- Annali dell'Istituto Superiore di Sanita, 2019, v. 55, n. 3, p. 265, doi. 10.4415/ANN_19_03_12
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- Article
DISTOMOLARUL – FRECVENºÅ, MANIFESTÅRI CLINICE ŞI ETIOLOGIE.
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- Romanian Journal of Stomatology / Revista Romana de Stomatologie, 2012, v. 58, n. 1, p. 68
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- Article
MEZIODENSUL FAMILIAL.
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- Romanian Journal of Stomatology / Revista Romana de Stomatologie, 2009, v. 55, n. 4, p. 293
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- Article
Can a mixed damage interfere with DNA-prottein cross-links repair?
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- Journal of Cellular & Molecular Medicine, 2001, v. 5, n. 2, p. 171, doi. 10.1111/j.1582-4934.2001.tb00150.x
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- Article
The Importance of Implementing a Transition Strategy for Patients with Muscular Dystrophy: From Child to Adult—Insights from a Tertiary Centre for Rare Neurological Diseases.
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- Children, 2023, v. 10, n. 6, p. 959, doi. 10.3390/children10060959
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- Article
Prenatal testing - a study on patients’ knowledge and attitude.
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- Ginecologia.ro, 2018, v. 6, n. 21, p. 6, doi. 10.26416/gine.21.3.2018.1944
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- Article
Diagnosticul și prevenţia preeclampsiei review de literatură.
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- Ginecologia.ro, 2017, v. 5, p. 39
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- Article
Testarea genetică prenatală neinvazivă prin AND liber fetal - metodă de screening pentru sarcinile cu risc înalt de malformaţii fetale.
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- Ginecologia.ro, 2017, v. 5, n. 16, p. 32
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- Article
Tendinţe actuale în testarea prenatală non-invazivă: ADN fetal liber.
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- Ginecologia.ro, 2016, v. 4, n. 12, p. 58
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- Article
Correlations between Demographic, Clinical, and Paraclinical Variables and Outcomes in Patients with KRAS-Mutant or KRAS Wild-Type Metastatic Colorectal Cancer—A Retrospective Study from a Tertiary-Level Center in Romania.
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- Diagnostics (2075-4418), 2023, v. 13, n. 18, p. 2930, doi. 10.3390/diagnostics13182930
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- Article
Challenging diagnoses of tetraploidy/diploidy and trisomy 12: utility of first-tier prenatal testing methods.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1258752
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- Article
Common, Rare, and Individual Oro-dental Findings in People with Down Syndrome.
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- Journal of International Oral Health, 2016, v. 8, n. 10, p. 964, doi. 10.4103/0976-7428.195211
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- Article
Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways—Case Report and Literature Review.
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- Genes, 2023, v. 14, n. 2, p. 433, doi. 10.3390/genes14020433
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- Article
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients.
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- Genes, 2021, v. 12, n. 7, p. 1025, doi. 10.3390/genes12071025
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- Article
Anesthetic Management of a Down Syndrome Patient with Subocclusive Syndrome.
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- Maedica - a Journal of Clinical Medicine, 2018, v. 13, n. 2, p. 159, doi. 10.26574/maedica.2018.13.2.159
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- Article
Endotracheal Intubation in a Down Syndrome Adult Undergoing Cataract Surgery - a Multidisciplinary Approach.
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- Maedica - a Journal of Clinical Medicine, 2017, v. 12, n. 2, p. 127
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- Article
Wolfram Syndrome Type I Case Report and Review—Focus on Early Diagnosis and Genetic Variants.
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- Medicina (1010660X), 2024, v. 60, n. 7, p. 1064, doi. 10.3390/medicina60071064
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- Article
Developments in Genetics: Better Management of Ovarian Cancer Patients.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 21, p. 15987, doi. 10.3390/ijms242115987
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- Article
Exploring the Literature on Narcolepsy: Insights into the Sleep Disorder That Strikes during the Day.
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- NeuroSci, 2023, v. 4, n. 4, p. 263, doi. 10.3390/neurosci4040022
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- Article
New changes in the classification of acute myeloid leukemia proposed by WHO 2022.
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- Oncolog-Hematolog, 2023, n. 65, p. 46
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- Article
"SHARE. CARE. CURE." - A EUROPEAN REFERENCE NETWORK FOR RARE INFECTIOUS DISEASES.
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- Romanian Archives of Microbiology & Immunology, 2021, v. 80, n. 4, p. 363, doi. 10.54044/rami.2021.04.08
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- Article