Search Results - "Rabbani, Ali"

Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants by Mahdieh, Nejat, Soveizi, Mahdieh, Tavasoli, Ali Reza, Rabbani, Ali, Ashrafi, Mahmoud Reza, Kohlschütter, Alfried, Rabbani, Bahareh

“…This study evaluates the genetic spectrum of leukodystrophies and leukoencephalopathies in Iran. 152 children, aged from 1 day to 15 years, were genetically…”
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Mesenchymal stem cell transplantation in newly diagnosed type-1 diabetes patients: a phase I/II randomized placebo-controlled clinical trial by Izadi, Mahmoud, Sadr Hashemi Nejad, Anavasadat, Moazenchi, Maedeh, Masoumi, Safdar, Rabbani, Ali, Kompani, Farzad, Hedayati Asl, Amir Abbas, Abbasi Kakroodi, Fatemeh, Jaroughi, Neda, Mohseni Meybodi, Mohammad Ali, Setoodeh, Aria, Abbasi, Farzaneh, Hosseini, Seyedeh Esmat, Moeini Nia, Fatemeh, Salman Yazdi, Reza, Navabi, Roghayeh, Hajizadeh-Saffar, Ensiyeh, Baharvand, Hossein

“…Abstract Background Type-1 diabetes (T1D) occurs following autoimmune-induced pancreatic beta cells death. Among several treatment modalities, mesenchymal stem…”
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E-Ink; Revolution of Displays by Ali Rabbani, Saghar, Ahmed, Maaz, Hashim Zahid, Abdullah

“…The emergence of digital technology has transformed the way we consume and interact with media, with one of the most significant innovations being the…”
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The Consensus on the Diagnosis and Management of Congenital Hypothyroidism in Term Neonates by Hashemipour, Mahin, Rabbani, Ali, Rad, Afagh Hassanzadeh, Dalili, Setila

“…Congenital hypothyroidism (CH) is one of the most treatable endocrine disorders in infants and children that can influence the function of many organs in the…”
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Tandem Mass Analysis of Amino Acids and Acylcarnitine Profiles in Neonates with Congenital Hypothyroidism by Lotfi, Jabar, Taghikhani, Mohammad, Rabbani, Ali, Khatami, Shohreh, Rasaee, Mohammad Javad

“…Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder. This study aimed to investigate whether disturbances in amino acid metabolism…”
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Extrinsic workforce diversity factors: An impact of employee characteristics on productivity by Ahsen Maqsoom, Muhammad Ali Musarat, Hasnain Mubbasit, Wesam Salah Alaloul, Hassan Ashraf, Muhammad Babar Ali Rabbani, Iram Shaheen

“…As the global population raises, developing countries seem to have issues with the productivity of the construction projects due to high demand. Therefore,…”
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The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants by Didban, Abdolah, Rabbani, Ali, Mahdieh, Nejat, Heshmatzad, Katayoun, Rabbani, Bahareh

“…Familial glucocorticoid deficiency is a rare autosomal recessive genetic disorder which belongs to a group of primary adrenal insufficiency (PAI) and is mainly…”
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Lignocellulosic fiber reinforcement in PPRC composites: An analysis of structural and thermal enhancements by Fahad Ali Rabbani, Yasin, Saima, Iqbal, Tanveer, Hamayoun Mahmood, Mujtaba, M A, Fouad, Yasser, Manzoore Elahi M. Soudagar, Kalam, M A

“…This study investigates the fabrication process of biocomposites and their resultant mechanical and thermal properties, essential for evaluating the…”
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Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b) by Eghbali, Maryam, Abiri, Maryam, Talebi, Saeed, Noroozi, Zahra, Shakiba, Marjan, Rostami, Parastoo, Alimadadi, Hosein, Najafi, Mehri, Yazarlou, Fatemeh, Rabbani, Ali, Modarressi, Mohammad Hossein

“…Glycogen storage disease (GSD) is a rare inborn error of the synthesis or degradation of glycogen metabolism. GSD1, the most common type of GSD, is categorized…”
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The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trial by Zarrabi, Morteza, Akbari, Masood Ghahvechi, Amanat, Man, Majmaa, Anahita, Moaiedi, Ali Reza, Montazerlotfelahi, Hadi, Nouri, Masoumeh, Hamidieh, Amir Ali, Badv, Reza Shervin, Karimi, Hossein, Rabbani, Ali, Mohebbi, Ali, Rahimi-Dehgolan, Shahram, Rahimi, Rosa, Dehghan, Ensieh, Vosough, Massoud, Abroun, Saeed, Shamsabadi, Farhad Mahvelati, Tavasoli, Ali Reza, Alizadeh, Houman, Pak, Neda, Zamani, Gholam Reza, Mohammadi, Mahmoud, Javadzadeh, Mohsen, Ghofrani, Mohammad, Hassanpour, Seyed Hossein, Heidari, Morteza, Taghdiri, Mohammad Mehdi, Mohseni, Mohamad Javad, Noparast, Zahra, Masoomi, Safdar, Goudarzi, Mehrdad, Mohamadpour, Masood, Shodjaee, Razieh, Samimi, Solaleh, Mohammad, Monireh, Gholami, Mona, Vafaei, Nahid, Koochakzadeh, Leyli, Valizadeh, Amir, Malamiri, Reza Azizi, Ashrafi, Mahmoud Reza

“…The current multi-center, randomized, double-blind study was conducted among children with cerebral palsy (CP) to assess the safety and efficacy of umbilical…”
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Experimental Study of Mechanical Properties of Polypropylene Random Copolymer and Rice-Husk-Based Biocomposite by Using Nanoindentation by Rabbani, Fahad Ali, Yasin, Saima, Iqbal, Tanveer, Farooq, Ujala

“…Nanoindentation is widely used to investigate the surface-mechanical properties of biocomposites. In this study, polypropylene random copolymer (PPRC) and…”
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In silico structural, functional and pathogenicity evaluation of a novel mutation: An overview of HSD3B2 gene mutations by Rabbani, Bahareh, Mahdieh, Nejat, Haghi Ashtiani, Mohammad Taghi, Setoodeh, Aria, Rabbani, Ali

“…Mutations of 3 beta hydroxysteroid dehydrogenase type II (HSD3B2) gene result in different clinical consequences. We explain a patient who demonstrated a salt…”
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Iranian Women’s Divorce Style: A Qualitative Study by Jaberi, Somayeh, Etemadi, Ozra, Fatehizade, Maryam, Rabbani Khorasgani, Ali

“…Divorce has received scant attention in Iran, despite the problems that arise for individuals and families and in social life. The present study aimed to find…”
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p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche by Rabbani, Ali, Bose, Himangshu S., Abbasi, Farzaneh, Sayarifard, Fatemeh, Setoodeh, Aria, Mahdieh, Nejat, Soveizi, Mahdieh, Rabbani, Bahareh

“…Premature pubarche (PP) is the appearance of sexual hair in children before puberty. The PP phenotype may attribute to nonclassic congenital adrenal…”
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The Role of Thyroid Function Tests in Diagnosing Allan-herndon-dudley Syndrome Revisited: A Novel Iran-based Mutation by Noorian, Shahab, Hamzehlou, Sepideh, Rabbani, Ali, Sotoudeh, Arya, Pour Rostami, Kioumars, Savad, Shahram

“…Introduction: Allan-Herndon-Dudley Syndrome (AHDS) is a rare X-linked recessive intellectual disability condition with neuromuscular involvements. Altered…”
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COVID-19: A New Horizon in Congenital Heart Diseases by Aghaei Moghadam, Ehsan, Mohammadzadeh, Shabnam, Sattarzadeh Badkoubeh, Roya, Ghamari, Azin, Rabbani, Ali, Mohebbi, Ali, Zeinaloo, Aliakbar, Ashrafi, Mahmoudreza, Kamran, Niyoosha, Masoominasab, Paniz, Mahmoudi, Zahra, Zamani Mehryan, Asma, Mirzaaghayan, Mohammad Reza

“…Previous studies have demonstrated that both children and adult patients with a history of congenital heart disease (CHD) are at high risk for coronavirus…”
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Novel Homozygous Mutation in the AGPAT2 Gene in a Child With Berardinelli-Seip Congenital Lipodystrophy Syndrome by Ahya Zaridoust, Rabbani, Ali, Hosseinverdi, Sima, Hilbert, Pascale, Rezaei, Nima

“…Berardinelli-Seip congenital lipodystrophy (BSCL) is an autosomal recessive disorder, characterized by the generalized absence of subcutaneous fat and muscular…”
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Enhancing MPPT Performance in Partially Shaded PV Systems under Sensor Malfunctioning with Fuzzy Control by Rabbani, Moazzam Ali, Qureshi, Muhammad Bilal, Al Qahtani, Salman A., Khan, Muhammad Mohsin, Pathak, Pranavkumar

“…The shift towards sustainable energy sources is gaining momentum due to their environmental cleanliness, abundant availability, and eco-friendly…”
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The Effect of Metformin as an Adjunct Therapy in Adolescents with Type 1 Diabetes by Setoodeh, Aria, Didban, Abdollah, Rabbani, Ali, Sayarifard, Azadeh, Abbasi, Farzaneh, Sayarifard, Fatemeh, Hoseinzade, Fatemeh

“…The strict control of blood glucose levels in adolescents with Type 1 Diabetes Mellitus (T1DM) is accompanied with a considerable long term decrease in…”
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Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village by Rowlands, Amanda, Deeb, Asma, Ladjouze, Asmahane, Hamza, Rasha T, Musa, Salwa A, Raza, Jamal, Jennane, Farida, Abu-Libdeh, Abdulsalam, Chanoine, Jean-Pierre, Fadila, Bouferoua, Hana, Delileche, Larbi, Djahlat, Mustapha, Noumi, Alkhayyat, Haya, Douksie, Abdourahman, Rabbani, Ali, Al-Jumaili, Ali, Odeh, Rasha, Alkandari, Hessa, Tfayli, Hala, Abusrewil, Suleiman, Ghawil, Millad, senani, Aisha Al, Abu-Libdeh, Abdulsalam, Alkhalaf, Fawziya, Habeb, Abdelhadi, Ahmad, Noman, Elshareef, Omer, Abdullah, Mohamed, Al-Hassan, Olivia, Karah, Dima, Hachicha, Mongia, Alshakka, Mohammed

“…Congenital adrenal hyperplasia (CAH), if untreated, carries high morbidity and mortality. A higher incidence of CAH is expected in countries where…”
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