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1دورية أكاديمية
المصدر: Journal of Clinical and Translational Endocrinology Case Reports, Vol 32, Iss , Pp 100165- (2024)
مصطلحات موضوعية: H syndrome, Infantile diabetes, Hypertrichosis, Hyperpigmentation, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Samaneh Noroozi Asl, Reza Ibrahimi, Sepideh Bagheri, Mojtaba Lotfi
المصدر: Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
مصطلحات موضوعية: 5‐Alpha reductase deficiency, dehydrotestosterone, disorder of sex development, Medicine, Medicine (General), R5-920
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2050-0904
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3دورية أكاديمية
المؤلفون: Nosrat Ghaemi, Martha Ghahraman, Samaneh Noroozi Asl, Rahim Vakili, Fatemeh Fardi Golyan, Meysam Moghbeli, Mohammad Reza Abbaszadegan
المصدر: Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-6 (2019)
مصطلحات موضوعية: Familial precocious puberty, GPR54 gene, Kisspeptin, Novel SNP, Pediatrics, RJ1-570
وصف الملف: electronic resource
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4
المؤلفون: Sara Nagy, Tracy Lau, Shahryar Alavi, Ehsan Ghayoor Karimiani, Jalal Vallian, Bobby G. Ng, Samaneh Noroozi Asl, Javad Akhondian, Amir Bahreini, Omid Yaghini, Prech Uapinyoying, Carsten Bonnemann, Hudson H. Freeze, Vajira H. W. Dissanayake, Nirmala D. Sirisena, Miriam Schmidts, Henry Houlden, Andres Moreno‐De‐Luca, Reza Maroofian
المصدر: Clinical Genetics. 102:530-536
مصطلحات موضوعية: Brain Diseases, Seizures, Intellectual Disability, Homozygote, Genetics, Humans, Membrane Proteins, Muscle, Skeletal, Mannosyltransferases, Genetics (clinical)
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5
المؤلفون: Samaneh Noroozi Asl, Reza Ibrahimi, Sepideh Bagheri, Mojtaba Lotfi
المصدر: Clinical Case Reports. 11
مصطلحات موضوعية: General Medicine
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6
المؤلفون: Hadis Ebrahimzadeh, Homa Ilkhanipoor, Fatemeh Sadat Mirrashidi, Daniel Zamanfar, Mahin Hashemipour, Nosrat Ghaemi, Fatemeh Aghamahdi, Atefeh Raoofat, Anis Amirhakimi, Somayyeh Hashemian, Hossein Moravej, Negar Yazdani, Peyman Eshraghi, Samaneh Noroozi Asl, Majid Vares Vazirian
المصدر: Primary Care Diabetes. 15:1100-1103
مصطلحات موضوعية: medicine.medical_specialty, endocrine system diseases, Referral, Endocrinology, Diabetes and Metabolism, Disease, Iran, Asymptomatic, Diabetes mellitus, Internal medicine, Internal Medicine, medicine, Humans, Family history, Referral and Consultation, Retrospective Studies, Type 1 diabetes, Nutrition and Dietetics, business.industry, nutritional and metabolic diseases, Retrospective cohort study, medicine.disease, Celiac Disease, Diabetes Mellitus, Type 1, Multicenter study, medicine.symptom, Family Practice, business
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7
المؤلفون: Peyman Eshraghi, Sepideh Bagheri, Vajiheh Chalak, Samaneh Noroozi Asl
المصدر: Journal of Pediatric Endocrinology and Metabolism. 32:885-888
مصطلحات موضوعية: Male, 0301 basic medicine, Pediatrics, medicine.medical_specialty, Phenylalanine, Endocrinology, Diabetes and Metabolism, Population, Iran, 030105 genetics & heredity, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Phenylketonurias, medicine, Humans, Phenylketonuria (PKU), Child, education, education.field_of_study, business.industry, Infant, Prognosis, medicine.disease, Biopterin, Diet, Clinical trial, Inborn error of metabolism, Child, Preschool, Pediatrics, Perinatology and Child Health, Female, business, Biomarkers, 030217 neurology & neurosurgery, Follow-Up Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0cc600f422c13b0c5331a787ec8c2e1
https://doi.org/10.1515/jpem-2018-0503 -
8
المؤلفون: Fahimeh Soheilipour, Mahin Hashemipour, Ghahramani S, De Franco E, Hanieh Yaghootkar, Samaneh Noroozi Asl, Rahim Vakili, Saba Vakili
المصدر: Journal of Pediatric Endocrinology and Metabolism. 32:607-613
مصطلحات موضوعية: Male, medicine.medical_specialty, Pediatrics, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Disease, Consanguinity, Iran, Osteochondrodysplasias, Infant, Newborn, Diseases, ABCC8, eIF-2 Kinase, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, 030225 pediatrics, Molecular genetics, Diabetes mellitus, Diabetes Mellitus, Humans, Medicine, EIF2AK3, Child, Genetic testing, biology, medicine.diagnostic_test, business.industry, Infant, Newborn, Prognosis, medicine.disease, Diabetes Mellitus, Type 1, Child, Preschool, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, Female, business, Epiphyses, Wolcott–Rallison syndrome, Biomarkers
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27cf11ff4df51ea1f5856d0eb7bf6d7f
https://doi.org/10.1515/jpem-2018-0434 -
9
المصدر: Journal of Neurology Research. 7:94-96
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::003c62c1d42d3189a4556218352cf1cb
https://doi.org/10.14740/jnr410e