Keywords: اختلافات خانوادگی; Familial dysautonomia; Sleep-disordered breathing; Polysomnography; SpO2; EtCO2;
مقالات ISI اختلافات 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: اختلافات خانوادگی; Autonomic neuropathy; Fabry's disease; Familial dysautonomia; Hypoventilation; Hereditary sensory and autonomic neuropathies;
Keywords: اختلافات خانوادگی; IKBKAP; inhibitor of kappa light polypeptide gene enhancer in B-cells; IKAP; IKK complex-associated protein; FD; familial dysautonomia; US; United States; CN; cranial nerve; CNS; central nervous system; MRI; magnetic resonance imaging; iPSC; induced pluri
Keywords: اختلافات خانوادگی; Familial dysautonomia; Blink reflex; Jaw jerk reflex; Afferent disorder; Hereditary sensory neuropathy; Hereditary sensory and autonomic neuropathy type III
Keywords: اختلافات خانوادگی; Catecholamine; Dopamine; Norepinephrine; Parkinson's disease; Neurodegeneration; AAG; autoimmune autonomic ganglionopathy; ALDH; aldehyde dehydrogenase; AMYL; amyloidosis; CAF; chronic autonomic failure; DA; dopamine; DHPG; 3,4-dihydroxyphenylglycol; DOPA
Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia
Keywords: اختلافات خانوادگی; ESR1; familial dysautonomia; IKBKAP; osteoporosis; VDR;
Founder mutation in IKBKAP gene causes vestibular impairment in familial dysautonomia
Keywords: اختلافات خانوادگی; Vestibular; Familial dysautonomia; IKBKAP; Gait ataxia; Hereditary sensory and autonomic neuropathy;
Proteasome inhibitors to alleviate aberrant IKBKAP mRNA splicing and low IKAP/hELP1 synthesis in familial dysautonomia
Keywords: اختلافات خانوادگی; Familial dysautonomia; Proteasome; Carfilzomib; IKBKAP; mRNA splicing; MicroRNA;
Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing
Keywords: اختلافات خانوادگی; Carrier screening; prenatal screening; autosomal recessive disorder; autosomal dominant disorder; X-linked disorder; thalassemia; hemoglobinopathy; cystic fibrosis; Duchenne/Becker muscular dystrophy; Fragile X; spinal muscular atrophy; Tay-Sachs disease;
Opinion commune de la SOGC et du CCGM sur le dépistage génétique en contexte de procréation : Mise à jour à l'intention de l'ensemble des prestataires canadiens de soins de santé maternelle et de services en procréation, à l'ère des tests offerts dire
Keywords: اختلافات خانوادگی; Carrier screening; prenatal screening; autosomal recessive disorder; autosomal dominant disorder; X-linked disorder; thalassemia; hemoglobinopathy; cystic fibrosis; Duchenne/Becker muscular dystrophy; Fragile X; spinal muscular atrophy; Tay-Sachs disease;
Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patients
Keywords: اختلافات خانوادگی; Familial dysautonomia; FD crisis; Stress; IKAP; IKBKAP; JNK; WBC; mRNA;
Familial dysautonomia (Riley–Day syndrome): When baroreceptor feedback fails
Keywords: اختلافات خانوادگی; Familial dysautonomia; Riley–Day syndrome; Hereditary sensory and autonomic neuropathy type III; Hypertension; Afferent baroreflex failure
Motility Problems in the Intellectually Challenged Child, Adolescent, and Young Adult
Keywords: اختلافات خانوادگی; Gastrointestinal motility disorders; Down syndrome; Cerebral palsy; Familial dysautonomia; Williams syndrome;
Enamel development in primary molars from children with familial dysautonomia
Keywords: اختلافات خانوادگی; Familial dysautonomia; Enamel; Hydroxyapatite; Primary molars
ELP3 localises to mitochondria and actin-rich domains at edges of HeLa cells
Keywords: اختلافات خانوادگی; FD; familial dysautonomia; ELP3; ELONGATOR 3; IKAP; I kappa B kinase complex-associated protein; Familial dysautonomia; Motor neuron disease; Amyotrophic lateral sclerosis; ELONGATOR; ELP3; Actin; Mitochondria;
Oral Self-Injurious Behaviors in Patients with Developmental Disabilities
Keywords: اختلافات خانوادگی; Self-injurious behavior; Self-injurious behaviors; Factitial injury; Intellectual disabilities; Developmental disabilities; Autism; Mental retardation; Lesch-Nyhan syndrome; Familial dysautonomia
A reinforced suture line prevents recurrence after fundoplication in patients with familial dysautonomia
Keywords: اختلافات خانوادگی; Gastroesophageal reflux; Nissen fundoplication; Familial dysautonomia;
Carrier Screening for Genetic Disorders in Individuals of Ashkenazi Jewish Descent
Keywords: اختلافات خانوادگی; Carrier Screening; Ashkenazi Jews; Canavan disease; Tay-Sachs disease; familial dysautonomia;
Dépistage des porteurs de troubles génétiques chez les personnes d'origine juive ahkénaze
Keywords: اختلافات خانوادگی; Carrier Screening; Ashkenazi Jews; Canavan disease; Tay-Sachs disease; familial dysautonomia;
Assessing Efficacy of High-Frequency Chest Wall Oscillation in Patients With Familial Dysautonomia
Keywords: اختلافات خانوادگی; antibiotic use; aspiration; familial dysautonomia; gastroesophageal reflux; hospitalizations; mucus; pneumonia; pulmonary function; secretionsATS = American Thoracic Society; FD = familial dysautonomia; GER = gastroesophageal reflux; HFCWO = high-frequenc
Tocotrienols reverse IKAP and monoamine oxidase deficiencies in familial dysautonomia
Keywords: اختلافات خانوادگی; Familial dysautonomia; IKAP; MAO A; Tocotrienol; EGCG;
New Insights into the Diagnosis and Treatment of Neurotrophic Keratopathy
Keywords: اختلافات خانوادگی; corneal nerves; corneal wound healing; diabetes mellitus; dry eye syndrome; familial dysautonomia; Gasserian ganglion; herpes simplex; herpes zoster ophthalmicus; ocular surgery; substance P;