Keywords: خانوادگی; Hepatocellular; Carcinoma; Familial; Hepatitis B; Prevention; Prognosis;
مقالات ISI خانوادگی (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: خانوادگی; Familial; Genetics; GWAS; Polygenic risk score; Testicular germ cell tumour;
Keywords: خانوادگی; Familial; Genetics; Whole exome sequencing; Hereditary; Multi-incident;
Keywords: خانوادگی; Hereditary; Renal cell carcinoma; Familial; VHL; Tuberous sclerosis; HLRCC; Immunohistochemistry; Cowden syndrome; HRPT2; Eosinophilic; Solid and cystic renal cell carcinoma;
Keywords: خانوادگی; Down syndrome; Alzheimer's disease; Familial; APP mutation; Biomarkers;
Keywords: خانوادگی; Bipolar disorder; High-risk; Familial; Cognition;
Keywords: خانوادگی; Hypermobility; Joint; Joint laxity; Familial; Questionnaires; Interview; Focus groups; Validity of results;
Keywords: خانوادگی; Bipolar disorder; Schizophrenia; Familial; Cognition; Relatives;
Keywords: خانوادگی; Bipolar disorder; Theory of mind; Familial; Cognition; Emotion recognition; Relatives;
Keywords: خانوادگی; Longevity; Cancer; Long-live parents; Familial; Parental longevity; Mortality; Socioeconomic status;
Keywords: خانوادگی; Familial; AVNRT; Tachycardia;
Keywords: خانوادگی; Schizophrenia; Genetic counseling; Familial; Risk;
Keywords: خانوادگی; Cerebral cavernous malformations; Diffuse manifestation; Familial; Prognosis;
Keywords: خانوادگی; Alcohol; Parental; Familial; Transmission; Sweden; Quantile regression;
Keywords: خانوادگی; Mirror neurons; Schizophrenia; Familial; Sporadic;
Keywords: خانوادگی; Pancreatic cancer; Risk factors; Familial; Smoking; Chronic pancreatitis;
Keywords: خانوادگی; adenoma; carcinoma; familial; familial hypocalciuric hypercalcemia; hereditary; hyperparathyroidism; hyperplasia; multiple endocrine neoplasia; parathyroid
Keywords: خانوادگی; Familial; Tumor suppressor; Pigmentation; Telomere;
Keywords: خانوادگی; Pancreatic cancer; Familial; Hereditary; Pathology; Morphology; Histology;
Keywords: خانوادگی; Osteochondritis dissecans; Genetic; Bilateral; Familial
Keywords: خانوادگی; Congenital malformation; Genetic; Molecular; Familial
Keywords: خانوادگی; idiopathic pulmonary fibrosis; genetics; familial; thrombocytopenia; myelodysplastic syndromes;
Keywords: خانوادگی; Hypertriglyceridemia; Children; Adolescents; Pancreatitis; Familial; Inherited
Keywords: خانوادگی; Hereditary; Familial; Syndrome; Pancreas; Cancer; Exocrine; Adenocarcinoma; Genetics;
Keywords: خانوادگی; Congenital; Familial; Subglottic; Stenosis;
Keywords: خانوادگی; Obsessive–compulsive disorder; Familial; Subtype; Paternal; Anxiety
Keywords: خانوادگی; SNCA; VPS35; PD; MSA; Genetics; Familial
Keywords: خانوادگی; Genetics of vascular malformations; Sporadic; Familial; Somatic mosaicism
Keywords: خانوادگی; Parkinsonism; Familial; Frontotemporal dementia; Genetics; Autosomal dominant; Mutation;
Keywords: خانوادگی; bipolar disorder; high risk; offspring; familial; disruptive mood dysregulation disorder;
Keywords: خانوادگی; cholestasis; familial; bile secretion; pruritus; childrenABC, ATP binding cassette; ASBT, apical sodium bile salt transporter; ATP, adenosine triphosphate; ATPase, adenosine triphosphatase; BRIC, benign recurrent intrahepatic cholestasis; BSEP, bile salt
Keywords: خانوادگی; Perry syndrome; DCTN1; Gene mutation; Respiratory insufficiency; Familial; Parkinsonism;
Keywords: خانوادگی; Essential tremor; Dystonia; Genetics; Familial; Clinical;
Keywords: خانوادگی; Essential tremor; Genetics; Familial; Clinical; Rate of progression;
Keywords: خانوادگی; Meniere's disease; Genetics; Familial; Family history;
Keywords: خانوادگی; Apolipoproteins; Chylomicronemia; Familial; Gene; Lipoprotein lipase; Lipoproteins; Orlistat;
Keywords: خانوادگی; Night Eating Syndrome; Familial; Genetic
Keywords: خانوادگی; Low back pain; Posture; Movement patterns; Familial; Classification
Evaluation of familial factors in a Mexican population-based setting with gastroschisis: Further evidence for an underlying genetic susceptibility
Keywords: خانوادگی; Familial; Gastroschisis; Genetics; Inheritance; Population-based; Recurrence;
Pulmonary Langerhans cell histiocytosis, acute myeloid leukemia, and myelofibrosis in a large family and review of the literature
Keywords: خانوادگی; Langerhans cell histiocytosis; Acute myeloid leukemia; Idiopathic myelofibrosis; Familial; Genetic;
Multiple endocrine neoplasia type 1: clinical correlates of MEN1 gene methylation
Keywords: خانوادگی; Methylation; MEN 1; parathyroid; familial;
Identification of a novel CTR9 germline mutation in a family with Wilms tumor
Keywords: خانوادگی; Wilms tumor; Familial; CTR9; Splice acceptor site; Diagnosis;
Protocolo diagnóstico de las miocardiopatÃas genéticas
Keywords: خانوادگی; MiocardiopatÃa; Genética; Familiar; Cardiomyopathy; Genetics; Familial;
Case ReportFamilial acute necrotizing encephalopathy with RANBP2 mutation: The first report in Northeast Asia
Keywords: خانوادگی; Acute necrotizing encephalopathy; RANBP2; Familial;
Familial small-intestine carcinoids: Chromosomal alterations and germline inositol polyphosphate multikinase sequencing
Keywords: خانوادگی; Carcinoid tumors; Familial; Neuroendocrine tumors; Small intestine;
Non-BRCA familial breast cancer: review of reported pathology and molecular findings
Keywords: خانوادگی; BRCAX; non-BRCA; breast pathology; oestrogen receptor; HER2-neu; basal; luminal; familial; family history;
Familial CEBPA-mutated acute myeloid leukemia
Keywords: خانوادگی; Familial; CEBPA; Acute myeloid leukemia; Germline; Mutation;
Maladie de Kikuchi-Fujimoto ou lymphadénite histiocytaire nécrosante : à propos de deux cas familiaux
Keywords: خانوادگی; Maladie de Kikuchi-Fujimoto; Familial; Hérédité; Lymphadénite histiocytaire nécrosante; Kikuchi-Fujimoto's disease; Familial; Heredity; Histiocytic necrotizing lymphadenitis;
Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS)
Keywords: خانوادگی; Mowat Wilson; Hirschsprung’s disease; Familial; Genetics; ZEB2 gene; Africa
Une hémorragie intravitréenne comme manifestation initiale de vitréorétinopathie exsudative familiale chez un enfant de huit ans
Keywords: خانوادگی; Familiale; Exsudative; Vitréorétinopathie; Intravitréen; Hémorragie; Pédiatrique; Familial; Exudative; Vitreoretinopathy; Vitreous; Hemorrhage; Pediatric;