Keywords: سندرم کالمن; HPG; hypothalamic-pituitary-gonadal; GnRH; gonadotropin-releasing hormone; FSH; follicle-stimulating hormone; LH; luteinizing hormone; CNS; central nervous system; HH; hypogonadotropic hypogonadism; PSA-NCAM; polysialic acid form of neural adhesion molecu
مقالات ISI سندرم کالمن (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 کالمن; GnRH; Gonadotropin Releasing Hormone; KS; Kallmann Syndrome; nIHH; normosmic idiopathic hypogonadotropic hypogonadism; IGD; isolated GnRH deficiency; LH; luteinizing hormone; FSH; follicle-stimulating hormone; CDP; constitutional delay of puberty; HA; hyp
Keywords: سندرم کالمن; Kallmann syndrome; Hypogonadism; Olfactory bulb; Olfaction Disorder; Magnetic resonance imaging; Syndrome de Kallmann; Hypogonadisme; Bulbe olfactif; Anosmie; Imagerie par résonnance magnétique;
Keywords: سندرم کالمن; fibroids; Mullerian aplasia; POF; OHSS; hypogonadism; Kallmann syndrome; PCOS; endometriosis;
Keywords: سندرم کالمن; human pluripotent stem cells; induced pluripotent stem cells; human embryonic stem cells; gonadotropin-releasing hormone; GnRH; puberty; hypogonadotropic hypogonadism; Kallmann syndrome
Keywords: سندرم کالمن; Accessory breasts; Kallmann syndrome; MRI
Keywords: سندرم کالمن; gonadotrophin; Kallmann syndrome; menarche; oestradiol; puberty; testosterone
Keywords: سندرم کالمن; Kallmann Syndrome; Psychosocial Factors; Body Image; Self-Esteem; Psychosexual Outcome; Nursing; Mixed Methods; Congenital Hypogonadotropic Hypogonadism
Keywords: سندرم کالمن; GnRH deficiency; Kallmann syndrome; hypogonadotrophic hypogonadism; male fertility; gonadotrophin therapy; fertility treatment; fertility outcomes
Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus
Keywords: سندرم کالمن; Anosmin-1; Cranial placode; Kallmann syndrome; Neural crest; Sensory organs; Xenopus;
Deficiency in GnRH receptor trafficking due to a novel homozygous mutation causes idiopathic hypogonadotropic hypogonadism in three prepubertal siblings
Keywords: سندرم کالمن; CDGP; constitutional delay of growth and puberty; CHO; Chinese hamster ovary; E2; estradiol; ER; endoplasmic reticulum; FSH; follicle-stimulating hormone; GnRH; gonadotropin-releasing hormone; HEK; human embryonic kidney; H-P-G axis; hypothalamic-pituit
Kallmann syndrome in pediatric otorhinolaryngology practice - Case report and literature review
Keywords: سندرم کالمن; Kallmann syndrome; Olfactory test; Anosmia; Hypogonadism;
A dominant negative FGFR1 mutation identified in a Kallmann syndrome patient
Keywords: سندرم کالمن; KS; Kallmann syndrome; IHH; isolated hypogonadotropic hypogonadism; FGFR1; fibroblast growth factor receptor 1; GnRH; gonadotropin-releasing hormone; PI3K; phosphiosidtide 3-linase; PLC; phospholipase C; PKC; protein kinase C; PCR; polymerase chain reacti
Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism
Keywords: سندرم کالمن; Hypogonadotropic hypogonadism; Kallmann syndrome; GnRH; Neuronal migration; Sense of smell and genes;
SÃndrome de Zinner en paciente afecto de sÃndrome de Kallmann: rara asociacion de 2 malformaciones embrionarias
Keywords: سندرم کالمن; SÃndrome de Zinner; SÃndrome de Kallmann; Dispareunia; AnomalÃas congénitas; Quiste de vesÃcula seminal; CirugÃa pélvica; Zinner syndrome; Kallmann syndrome; Dyspareunia; Congenital abnormalities; Seminal vesicle cyst; Pelvis surgery;
Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene
Keywords: سندرم کالمن; Isolated gonadotropin-releasing hormone deficiency; Kallmann syndrome; KAL1 mutations; Clinical phenotype
Snapin interacts with G-protein coupled receptor PKR2
Keywords: سندرم کالمن; PKR2; Snapin; Yeast two hybrid; G-protein coupled receptor; GFP; green fluorescence protein; GnRH; gonadotropin-releasing hormone; GPCRs; G protein-coupled receptors; GST; glutathione S-transferase; IHH; idiopathic hypogonadotropic hypogonadism; KS; Kallm
Research reportPerinatal midline astrocyte development is impaired in fibroblast growth factor 8 hypomorphic mice
Keywords: سندرم کالمن; Fibroblast growth factor 8; Glial fibrillary acidic protein; Kallmann syndrome; Agenesis of the corpus callosum;
Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome
Keywords: سندرم کالمن; Next generation DNA sequencing; Kallmann syndrome; Hypogonadotropic hypogonadism; Delayed puberty; GnRH deficiency;
Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform
Keywords: سندرم کالمن; Hypogonadotropic hypogonadism; Kallmann syndrome; FGFR1; KAL2; genetics;
Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD)
Keywords: سندرم کالمن; Luciferase assay; Septo-optic dysplasia; KAL1; Kallmann syndrome; Females;
The Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system
Keywords: سندرم کالمن; Olfactory development; Neuronal differentiation; microRNA; GnRH; Dlx; Foxg1; Kallmann syndrome;
Brain anatomical substrates of mirror movements in Kallmann syndrome
Keywords: سندرم کالمن; Kallmann syndrome; Mirror movements; MRI; Brain; Motor cortex;
Genetics of congenital hypogonadotropic hypogonadism in Denmark
Keywords: سندرم کالمن; CHARGE syndrome; Congenital hypogonadotropic hypogonadism; Kallmann syndrome; Puberty
The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome
Keywords: سندرم کالمن; KAL1; Kallmann syndrome; male infertility; mutation; SNP;
Identification of HESX1 mutations in Kallmann syndrome
Keywords: سندرم کالمن; HESX1; Kallmann syndrome; hypogonadotropic hypogonadism; delayed puberty; GnRH deficiency;
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
Keywords: سندرم کالمن; Kallmann syndrome; KAL1 abnormalities; MLPA; KALP spurious amplification
Síndrome de Kallmann… será possível um diagnóstico mais precoce?
Keywords: سندرم کالمن; Atraso pubertário; Hipogonadismo hipogonadotrófico; Anosmia; Síndrome de Kallmann; MalformaçõesPuberty delay; Hypogonadotrophic hypogonadism; Anosmia; Kallmann Syndrome; Associated anomalies
Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome
Keywords: سندرم کالمن; FGFR1; Kallmann syndrome; KAL2; skeletal malformations
A fertile male patient with Kallmann syndrome and two missense mutations in the KAL1 gene
Keywords: سندرم کالمن; Kallmann syndrome; mutation; KAL1; fertility;
The puzzles of the prokineticin 2 pathway in human reproduction
Keywords: سندرم کالمن; Prokineticin 2; Prokineticin 2 receptor; GnRH deficiency; GnRH neuronal ontogeny; Kallmann syndrome; Hypogonadotropic hypogonadism
Role of fibroblast growth factor (FGF) signaling in the neuroendocrine control of human reproduction
Keywords: سندرم کالمن; GnRH deficiency; Kallmann syndrome; FGF signaling; FGFR1; FGF8; Oligogenicity
X-linked GnRH deficiency: Role of KAL-1 mutations in GnRH deficiency
Keywords: سندرم کالمن; GnRH deficiency; Kallmann syndrome; Anosmin-1; FGF signalling
Genetic counseling for isolated GnRH deficiency
Keywords: سندرم کالمن; Genetic counseling; GnRH deficiency; Kallmann syndrome
Isolated GnRH deficiency: A disease model serving as a unique prism into the systems biology of the GnRH neuronal network
Keywords: سندرم کالمن; GnRH; GnRH deficiency; GnRH neuronal ontogeny; Puberty; Kallmann syndrome; Hypogonadotropic hypogonadism
Estradiol levels in men with congenital hypogonadotropic hypogonadism and the effects of different modalities of hormonal treatment
Keywords: سندرم کالمن; Estradiol; androgens; testosterone; hypogonadotropic hypogonadism; Kallmann syndrome; Klinefelter syndrome; osteoporosis;
Estimation of instantaneous secretory rates and intrinsic characteristics of luteinizing hormone secretion in women with Kallmann syndrome before and after estriol administration
Keywords: سندرم کالمن; Kallmann syndrome; LH pulses; estriol treatment;
The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
Keywords: سندرم کالمن; CHARGE syndrome; CHD7 gene; Idiopathic hypogonadotropic hypogonadism; Kallmann syndrome; GnRH neuron; Anosmia
The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome
Keywords: سندرم کالمن; Digenic mutations; idiopathic hypogonadotropic hypogonadism; Kallmann syndrome;
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome
Keywords: سندرم کالمن; Nasal embryonic LHRH factor; hypogonadotropic hypogonadism; Kallmann syndrome; gonadotropin-releasing hormone (GnRH); GnRH neuron migration;
Kallmann syndrome and mirror movements: White matter quantitative evaluation with magnetic resonance imaging
Keywords: سندرم کالمن; Kallmann syndrome; Synkinesis; Magnetic resonance imaging; Quantitative evaluation
Congenital hypogonadotropic hypogonadism in females: Clinical spectrum, evaluation and genetics
Keywords: سندرم کالمن; Hypogonadisme hypogonadotrope congénital de la femme; Anosmie; Syndrome de Kallmann; Aménorrhée; GnRH; InfertilitéCongenital hypogonadotropic hypogonadism in women; Anosmia; Kallmann syndrome; Amenorrhea; GnRH; Gonadotropins
Genetic determinants of pubertal timing in the general population
Keywords: سندرم کالمن; Puberty; Pubertal timing; Genetics; Hypogonadotropic hypgonadism; Kallmann syndrome; Genetic regulation
Genetics basis for GnRH-dependent pubertal disorders in humans
Keywords: سندرم کالمن; Kallmann syndrome; Isolated hypogonadotropic hypogonadism; Central precocious puberty; GnRH neurons; Kisspeptin
An Unusual Case of Autonomous Hyperparathyroidism in a Patient With X-Linked Hypophosphatemic Rickets and Kallmann Syndrome
Keywords: سندرم کالمن; Hyperparathyroidism; Hypophosphatemic rickets; Kallmann syndrome;
Anosmin-1a is required for fasciculation and terminal targeting of olfactory sensory neuron axons in the zebrafish olfactory system
Keywords: سندرم کالمن; Anosmin-1; Kallmann syndrome; Olfactory system; Zebrafish; Kal1a gene
Essential requirement for zebrafish anosmin-1a in the migration of the posterior lateral line primordium
Keywords: سندرم کالمن; Anosmin-1; Kallmann syndrome; Kal1a gene; Zebrafish; Cell migration; Posterior Lateral line primordium; SDF1a
Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome
Keywords: سندرم کالمن; Kallmann syndrome; KAL1; hypogonadotropic hypogonadism; renal agenesis; renal dysgenesis; ichthyosis
Localization of anosmin-1a and anosmin-1b in the inner ear and neuromasts of zebrafish
Keywords: سندرم کالمن; Zebrafish; Kallmann syndrome; Kal1a; Kal1b; Anosmin-1a; Anosmin-1b; Neuromast; Inner ear; Hair cells; Kinocilia; Stereocilia; Lateral line; Crista; Anosmia; Hypogonadism; Anti-anosmin-1a; Anti-anosmin-1b; Scanning electron microscopy
Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1)
Keywords: سندرم کالمن; Kallmann syndrome; Fibroblast growth factor receptor 1; Children