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فیلتر نتایج
Setyed mehdi Kalantar
Mehrdad Noruzinia
نتایج 1 تا 10 از مجموع 20
1
2
Journal Paper
A Novel Heterozygous Pathogenic Mutation of PPP۲RIA Gene in a Pediatric Encephalopathy Patient: A Case Report
Authors:
Hassan Bakhtiary
،
Narges Heidari
Year 1402
Publish place:
Journal of Advances in Medical and Biomedical Research Issue 149، Vol 31
Pages:
5
| Language: English
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Journal Paper
Evaluation of the Genetic Background of Patients with Niemann-Pick Disease
Authors:
Fatemeh Alipouran
،
Ehsan Ghayoor Karimiani
،
Jina Khayatzadeh
Year 1402
Publish place:
Reports of Biochemistry and Molecular Biology Issue 3، Vol 12
Pages:
7
| Language: English
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Journal Paper
Coffin-Lowry Syndrome: The First Molecularly Confirmed Report in Iran
Authors:
Ali Nikfar
،
Mojdeh Mansouri
،
Gita Fatemi Abhari
Year 1397
Publish place:
Iranian Rehabilitation Journal Issue 3، Vol 16
Pages:
5
| Language: English
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Journal Paper
بررسی ژنتیکی کاردیومیوپاتی هایپرتروفیک در بیماران ایرانی؛ نقش یک جهش نوپدید
Authors:
ارسطو کاکی
،
محمد دلیلی
،
نجات مهدیه
،
مهرداد نوروزی نیا
Year 1402
Publish place:
Pajouhan Scientific Journal Issue 3، Vol 21
Pages:
8
| Language: Persian
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Journal Paper
A Missense Mutation in the HMNT Gene Responsible for Autosomal Recessive Intellectual Disability in an Iranian Family with Consanguineous Marriage
Authors:
سید حمیدرضا میرابوطالبی
،
محمدرضا دهقانی
،
نسرین قاسمی
،
محمد یحیی وحیدی مهرجردی
،
مجتبی موحدی نیا
،
سید مهدی کلانتر
Year 1401
Publish place:
International Journal of Medical Laboratory Issue 3، Vol 9
Pages:
8
| Language: English
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Journal Paper
A Compound Heterozygous HPD Mutation in an Iranian Patient with Hypertyrosinemia Type III
Authors:
فاطمه سرکارگر
،
سیدعلی مدنی
،
احسان زارع مهرجردی
،
حسین خدایی
،
سیدمهدی کلانتر
،
سیداحمد محمدی
Year 1401
Publish place:
International Journal of Medical Laboratory Issue 4، Vol 9
Pages:
6
| Language: English
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Journal Paper
Novel WDR۶۲ and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-۲ With Polymicrogyria and Homocystinuria-Megaloblastic Anemia
Authors:
Tahereh Dianat
،
Dor Mohammad Kordi Tamandani
،
Maryam Najafi
،
Ali Khajeh
Year 1401
Publish place:
Disease and Diagnosis Issue 4، Vol 11
Pages:
5
| Language: English
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Journal Paper
Wiedemann-Steiner Syndrome with a ۲-Year Follow-Up
Authors:
Mohamad Hosein Mohamadi
،
Moein Mobini
،
Saba Vakili
،
Rahim Vakili
Year 1401
Publish place:
International Journal of Pediatrics Issue 10، Vol 10
Pages:
6
| Language: English
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Journal Paper
A substitution mutation in LRP۸ gene is significantly associated with susceptibility to familial myocardial infarction
Authors:
Mohammad Javad Ghorbani
،
Nematollah Razmi
،
Seyed Mohammad Bagher Tabei
،
Mohammad Javad Zibaeenezhad
،
Hamid Reza Goodarzi
Year 1399
Publish place:
ARYA Atherosclerosis Issue 6، Vol 16
Pages:
5
| Language: English
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Journal Paper
Inconsistency in the expression pattern of a five-lncRNA signature as a potential diagnostic biomarker for gastric cancer patients in bioinformatics and in vitro
Authors:
Mahmoud Ghanei
،
Arash Poursjeikhani
،
Azadeh Aarabi
،
Negin Taghehchian
،
Mohammad Reza Abbaszadegan
Year 1401
Publish place:
Iranian Journal of Basic Medical Sciences Issue 6، Vol 25
Pages:
11
| Language: English
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نتایج 1 تا 10 از مجموع 20
1
2