Keywords: سندرم LEOPARD; LEOPARD syndrome; ventricular septal hypertrophy; arrhythmia; anesthesia;
مقالات ISI سندرم LEOPARD (ترجمه نشده)
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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: سندرم LEOPARD; Noonan syndrome; LEOPARD syndrome; Lentigines; Giant cell tumor; Giant cell granuloma; Mandible; Maxilla
Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies
Keywords: سندرم LEOPARD; RAS signaling; RASopathies; Noonan syndrome; LEOPARD syndrome; Costello syndrome; Genotype-phenotype correlations; Congenital heart defect; Hypertrophic cardiomyopathy;
Determination of the catalytic activity of LEOPARD syndrome-associated SHP2 mutants toward parafibromin, a bona fide SHP2 substrate involved in Wnt signaling
Keywords: سندرم LEOPARD; SHP2/PTPN11; LEOPARD syndrome; Noonan syndrome; Protein tyrosine phosphatase; Parafibromin/CDC73; Wnt signal; SHP2; Src homology 2 domain-containing protein tyrosine phosphatase 2; PTP; Protein tyrosine phosphatase; NS; Noonan syndrome; LS; LEOPARD syndro
An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease
Keywords: سندرم LEOPARD; Neurofibromatosis type 1; Cafe-au-lait spots; Ephelids; Freckling; Neurofibroma; Legius syndrome; RASopathies; LEOPARD syndrome; Albinism; NeurofibrominNeurofibromatosis tipo 1; Mancha café con leche; Efélides; Pecas; Neurofibroma; Síndrome de Legius; Ras
Síndrome LEOPARD sin sordera ni estenosis pulmonar: a propósito de 2 casos
Keywords: سندرم LEOPARD; Rasopatia; Manchas café con leche; Lentigines; Sindrome LEOPARDRasopathy; Cafe au lait macules; Lentigines; LEOPARD syndrome
SÃndrome cardiofaciocutáneo, un trastorno relacionado con el sÃndrome de Noonan: hallazgos clÃnicos y moleculares en 11 pacientes
Keywords: سندرم LEOPARD; SÃndrome de Noonan; SÃndrome cardiofaciocutáneo; SÃndrome LEOPARD; Estenosis pulmonar valvular; MiocardiopatÃa hipertrófica; VÃa RAS-MAPK; RasopatÃa; PTPN11; BRAF; MAP2K1; Correlación genotipo-fenotipo; Noonan syndrome; Cardiofaciocutaneous syndr
Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: Clinical and molecular findings in 11 patients
Keywords: سندرم LEOPARD; Noonan syndrome; Cardiofaciocutaneous syndrome; LEOPARD syndrome; Pulmonary valve stenosis; Hypertrophic cardiomyopathy; RAS-MAPK pathway; Rasopathy; PTPN11; BRAF; MAP2K1; Genotype–phenotype correlationSíndrome de Noonan; Síndrome cardiofaciocutáneo; Sínd
The case of 17-year-old male with LEOPARD syndrome
Keywords: سندرم LEOPARD; LEOPARD syndrome; Mutation; Cardiomyopathy; Lentigines
Síndrome LEOPARD: una variante del síndrome de Noonan con fuerte asociación a miocardiopatía hipertrófica
Keywords: سندرم LEOPARD; SL, síndrome LEOPARD; SN, síndrome de Noonan; SNCFC, síndromes neurocardiofaciocutáneosSíndrome de Noonan; Síndrome LEOPARD; Lentiginosis múltiple; Miocardiopatía hipertrófica; Genes RAS-MAPKNoonan syndrome; LEOPARD syndrome; Multiple lentigines; Hypertro
LEOPARD Syndrome: A Variant of Noonan Syndrome Strongly Associated With Hypertrophic Cardiomyopathy
Keywords: سندرم LEOPARD; LS, LEOPARD syndrome; NCFCS, neurocardiofaciocutaneous syndromes; NS, Noonan syndromeNoonan syndrome; LEOPARD syndrome; Multiple lentigines; Hypertrophic cardiomyopathy; RAS-MAPK genesSíndrome de Noonan; Síndrome LEOPARD; Lentiginosis múltiple; Miocardiop
Spectrum of Mutations in Noonan Syndrome and Their Correlation with Phenotypes
Keywords: سندرم LEOPARD; CFC; Cardiofaciocutaneous syndrome; CR2; Converted region 2; CS; Costello syndrome; EGF; Epidermal growth factor; HF; Histone-like folds; LS; LEOPARD syndrome; MAPK; Mitogen-activated protein kinase; NS; Noonan syndrome;
Noonan syndrome and clinically related disorders
Keywords: سندرم LEOPARD; Noonan syndrome; LEOPARD syndrome; Noonan-like syndrome with loose anagen hair; CBL mutation-associated syndrome; RAS signaling; pathogenetic mechanisms; diagnosis; patient management; genotype-phenotype correlations
Novel BRAF mutation in a patient with LEOPARD syndrome and normal intelligence
Keywords: سندرم LEOPARD; Noonan syndrome; LEOPARD syndrome; Cardio-facio-cutaneous syndrome; Mitogen-activated protein kinases; BRAF
La voie de signalisation de RAS et ses syndromes (Noonan, LEOPARD, CFC, Costello)
Keywords: سندرم LEOPARD; Syndrome de Noonan; Syndrome LEOPARD; Syndrome CFC; Syndrome de Costello; Noonan syndrome; LEOPARD syndrome; PTPN11 protein; human; Syndrome;
Germ-line and somatic PTPN11 mutations in human disease
Keywords: سندرم LEOPARD; PTPN11; SHP-2; Noonan syndrome; LEOPARD syndrome; Juvenile myelomonocytic leukemia; Acute leukemia; Myelodysplastic syndromes; Gain-of-function mutations; Genotype-phenotype correlation;