Keywords: دیسپلازی سپتو-اپتیک; ACTH; adrenocorticotropin hormone; ALGS; arteriohepatic dysplasia; CH; central hypothyroidism; DWS; Dandy-Walker syndrome; FT3; free triiodothyronine; FT4; free thyroxine; GH; growth hormone; HCG; human chorionic gonadotropin; IGDF1; immunogobulin superfa
مقالات ISI دیسپلازی سپتو-اپتیک (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: دیسپلازی سپتو-اپتیک; Optic nerve hypoplasia; Septo-optic dysplasia; Epidemiology; Hypopituitarism; Hypothalamic-pituitary dysfunction; Clinical presentation; Diagnosis; Management;
Keywords: دیسپلازی سپتو-اپتیک; Septo-optic dysplasia; Optic nerve hypoplasia; Hypopituitarism; Autism; Autistic spectrum disorders; Blindness; Visual impairment;
MRI measurements of the normal pediatric optic nerve pathway
Keywords: دیسپلازی سپتو-اپتیک; Pediatric MRI; Optic pathway; Optic nerve hyperplasia; Septo-optic dysplasia; Krabbe's disease;
Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital Hypopituitarism
Keywords: دیسپلازی سپتو-اپتیک; cholestasis; congenital hypopituitarism; septo-optic dysplasia; canalicular ectoenzymes; canalicular transport proteins; ACTH; Adrenocorticotropic hormone; BSEP; Bile salt export pump; CD13; Alanyl aminopeptidase; FIC1; Familial intrahepatic cholestasis t
Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study
Keywords: دیسپلازی سپتو-اپتیک; Septo-optic dysplasia; Prevalence; Population based; Maternal age; Associated anomalies; EUROCAT;
Case ReportSix adult patients with septo-optic dysplasia and drug-resistant epilepsy: Clinical findings and courseâ
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Keywords: دیسپلازی سپتو-اپتیک; Septo-optic dysplasia; Seizures; Epilepsy; Drug-resistant; Cortical malformation; Seizure surgery;
Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD)
Keywords: دیسپلازی سپتو-اپتیک; Luciferase assay; Septo-optic dysplasia; KAL1; Kallmann syndrome; Females;
Congenital mydriasis as an initial sign of septo-optic dysplasia
Keywords: دیسپلازی سپتو-اپتیک; Agenesis septum pellucidum; Impaired neuronal migration; Amaurosis; Septo-optic dysplasia; Optic nerve hypoplasia; Mydriasis; Congenital mydriasis; Morsier syndrome; Agenesia septum pellucidum; Alteración migración neuronal; Amaurosis; Displasia septo-Ã
Prenatal determinants of optic nerve hypoplasia: Review of suggested correlates and future focus
Keywords: دیسپلازی سپتو-اپتیک; optic nerve hypoplasia; septo-optic dysplasia; epidemiology; hypopituitarism; maternal age; prenatal risk factors; birth defect
Septo-optic dysplasia and other midline defects: The role of transcription factors: HESX1 and beyond
Keywords: دیسپلازی سپتو-اپتیک; Septo-optic dysplasia; pituitary; HESX1; SOX2; SOX3; OTX2
Magnetic resonance virtual histology for embryos: 3D atlases for automated high-throughput phenotyping
Keywords: دیسپلازی سپتو-اپتیک; dpc; days post coitum; MRI; magnetic resonance imaging; OPT; optical projection tomography; μCT; microscopic computed tomography; DTI; diffusion tensor imaging; CNS; central nervous system; Gd-DTPA; gadolinium-diethylene-triamine-pentaacetic acid; VBM; v
Two cases of septo-optic dysplasia-plus syndrome with epilepsy and mirror hand movements
Keywords: دیسپلازی سپتو-اپتیک; Septo-optic dysplasia; Epilepsy; Skeletal malformations; Central nervous system abnormalities; Mirror movements; MRI findings
The subclassification of schizencephaly and its clinical characterization
Keywords: دیسپلازی سپتو-اپتیک; Schizencephaly; Septo-optic dysplasia; Optic nerve hypoplasia; Absence of the septum pellucidum; Polymicrogyria; Bilateral perisylvian syndrome
DNMT1 interacts with the developmental transcriptional repressor HESX1
Keywords: دیسپلازی سپتو-اپتیک; aa; amino acid; DNMT1; DNA methyltransferase 1; SAFB1; scaffold attachment factor beta 1; RNF2; ring finger protein 2; Lonp2; lon peptidase 2, peroxisomal; ZFP592; zinc finger protein 592; BTBD2; BTB (POZ) domain containing 2; SRFBP1; serum response facto
Developmental disorders of the hypothalamus and pituitary gland associated with congenital hypopituitarism
Keywords: دیسپلازی سپتو-اپتیک; pituitary; septo-optic dysplasia; isolated GHD; combined pituitary hormone deficiency; transcription factors