Electrochemical oxidation of catechol in the presence of 2-thiouracil: application to electro-organic synthesis von Shahrokhian, Saeed, Hamzehloei, Ali

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Chromium(III) Porphyrin as a Selective Ionophore in a Salicylate-Selective Membrane Electrode von Shahrokhian, Saeed, Hamzehloei, Ali, Bagherzadeh, Mojtaba

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Electrocatalytic Oxidation of 2-Thiouracil and 2-Thiobarbituric Acid at a Carbon-Paste Electrode Modified with Cobalt Phthalocyanine von Shahrokhian, Saeed, Hamzehloei, Ali, Thaghani, Abdollah, Mousavi, S. Reza

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Quantitative Analysis of capsaicin in Capsicum frutescens L. by 1HNMR von Nazari, F, Nejad Ebrahimi, S, Talebi, M, Kazemizadeh, Z, Hamzehloei, A, Shabani, S

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Potentiometric membrane sensors based on zirconyl(IV) phthalocyanine for detection of sulfosalicylic acid von Shahrokhian, Saeed, Taghani, Abdollah, Hamzehloei, Ali, Reza Mousavi, S.

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Electrooxidation of Iodide in the Presence of 4-Hydroxycoumarin: Application to a Simple Coulometric Titration of 4-Hydroxycoumarin von NEMATOLLAHI, Davood, HAMZEHLOEI, Ali, HESARI, Mehdi, RAHIMI, Javad

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Electrochemical Study of Iodide in the Presence of 2-Thiobarbituric Acid-Catalytic Determination of 2-Thiobarbituric Acid von Davood Nematollahi, Javad Rahimi, Mehdi Hesari, Ali Hamzehloei

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Tetrahydrobiopterin responsiveness in Phenylalanine hydroxylase deficient patients from North-east of Iran: Genotype-phenotype correlation, identification of a novel mutation and 7... von Khaghani, Faeze, Eshraghi, Peyman, Hamzehloei, Tayebeh

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Effects of carvacrol and physical exercise on motor and memory impairments associated with Parkinson's disease von Hamzehloei, Leila, Rezvani, Mohammad Ebrahim, Rajaei, Ziba

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Identified PAH V230A and PAH V230I mutations in a family with diverse clinical presentations von Khaghani, Faeze, Eshraghi, Peyman, Hamzehloei, Tayebeh

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Electrochemical determination of Clozapine on MWCNTs/New Coccine doped PPY modified GCE: An experimental design approach von Shahrokhian, Saeed, Kamalzadeh, Zahra, Hamzehloei, Ali

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Examining the Ramifications of the Expanding Domain of Public Law in Iran's Legal Framework von Hassan Hamzehloei, Maghsood Ranjbar, Mohammad Taghi Dashty

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Generation of Zebrafish Models of Human Retinitis Pigmentosa Diseases Using CRISPR/Cas9-Mediated Gene Editing System von Mirzaei, Farzaneh, Eslahi, Atiyeh, Karimi, Sareh, Alizadeh, Farzaneh, Salmaninejad, Arash, Rezaei, Mohammad, Mozaffari, Sina, Hamzehloei, Tayebeh, Pasdar, Alireza, Mojarrad, Majid

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Micronutrients intake and genetic variants associated with premature ovarian insufficiency; MASHAD cohort study von Mirinezhad, Mohammad Reza, Aghsizadeh, Maliheh, Ghazizadeh, Hamideh, Ghoflchi, Sahar, Bidary, Mohammad Zamiri, Naghipour, Alireza, Ferns, Gordon A, Hamzehloei, Tayebeh, Pasdar, Alireza, Ghayour-Mobarhan, Majid

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Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease‐causing variants von Sadat Fatemi, Seyedeh Helia, Eshraghi, Peyman, Ghanei, Mahmoud, Hamzehloei, Tayebeh

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Corrigendum to: An investigation of cystic fibrosis common mutations among Baluch ethnic minority in Iran [Gene Rep vol. 25 (2021) 101330] von Noori, Noor Mohammad, Jalali, Elaheh, Hamzehloei, Tayebeh, Shahraki, Touran

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Association between Genetic Variants Linked to Premature Ovarian Insufficiency and Inflammatory Markers: A Cross-Sectional Study von Mirinezhad, Mohammad Reza, Aghsizadeh, Maliheh, Fazl Mashhadi, Mohammadreza, Moazedi, Sara, Mohammadi Bajgiran, Maryam, Ghazizadeh, Hamideh, Yaghouti, Shayan, Mohammadian Ghosooni, Mahdi, Mohammadi, Mohammad Amin, Hasanzadeh, Elahe, Ebrahimi Dabagh, Ali, Rastegarmoghadam Ebrahimian, Arezoo, Akbarpour, Ensieh, Esmaily, Habibollah, Ferns, Gordon A, Hamzehloei, Tayebeh, Pasdar, Alireza, Ghayour-Mobarhan, Majid

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An investigation of cystic fibrosis common mutations among Baluch ethnic minority in Iran von Noori, Noor Mohammad, Jalali, Elaheh, Hamzehloei, Tayebeh, Shahraki, Touran

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Coincident APC point mutation and germline rearrangement in an Iranian polyposis family with an unusually severe phenotype von Tayebeh, Hamzehloei, Abdolazim, Sarli

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Mutation screening of whole PAH gene in the PKU patients from North east of Iran von Tayebeh, Hamzehloei, Amir, Hoseini

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