Chronic inflammation: Cross linking insights from Ayurvedic Sciences, a silver lining to systems biology and personalized medicine von Nair, Pratibha P., Krishnakumar, V, Nair, Parvathy G.

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Consanguinity and reproductive health among Arabs von Tadmouri, Ghazi O, Nair, Pratibha, Obeid, Tasneem, Al Ali, Mahmoud T, Al Khaja, Najib, Hamamy, Hanan A

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Development and validation of a questionnaire (SOMA-Q) to assess ojus in manasroga von Febin, H, Madhavan, Jithesh, Pratibha, Nair

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An Ayurvedic personalized prophylactic protocol in COVID-19 von Nair, Pratibha P., Nair, Parvathy G., Pratap Shankar, K.M.

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Ayurvedic management of neurological deficits post COVID-19 vaccination - A report of two cases von Pratap Shankar, K.M., Pratibha, P. Nair, Saritha, V.

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Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database von Bizzari, Sami, Nair, Pratibha, Hana, Sayeeda, Deepthi, Asha, Al-Ali, Mahmoud Taleb, Al-Gazali, Lihadh, El-Hayek, Stephany

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Ayurvedic practice, education and research, beyond dilemmas and confessions von Pratibha, Nair, E, Mukesh, Mv, VinodKumar

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Can the vagus nerve serve as biomarker for vata dosha activity? von Sumantran, Venil N., Nair, Pratibha P.

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Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case report von Bastaki, Fatma, Nair, Pratibha, Mohamed, Madiha, Malik, Ethar Mustafa, Helmi, Mustafa, Al-Ali, Mahmoud Taleb, Hamzeh, Abdul Rezzak

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A case report on probable short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing following vairechanika nasya in Ménière's disease von Krishna Kumar, V., Nair, Pratibha P., Sree Deepthi, G.N., Pradeep Kumar, P.P.

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Evaluating the Impact of Outpatient Multi-Dose Medication Packaging Service (MDMPS) on Medication Adherence and Clinical Outcomes von Nair, Pratibha, Kee, Kok Wai, Mah, Choon Siong, Lee, Eng Sing

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Characterization of an Emirati TMEM138 mutation leading to Joubert syndrome von Bizzari, Sami, Hamzeh, Abdul Rezzak, Nair, Pratibha, Mohamed, Madiha, Bastaki, Fatma

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A Novel Variant in the Endothelin-Converting Enzyme-Like 1 (ECEL1) Gene in an Emirati Child von Hamzeh, Abdul Rezzak, Nair, Pratibha, Mohamed, Madiha, Saif, Fatima, Tawfiq, Nafisa, Khalifa, Mohamed, Al-Ali, Mahmoud Taleb, Bastaki, Fatma

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Novel splice-site mutation in WDR62 revealed by whole-exome sequencing in a Sudanese family with primary microcephaly von Bastaki, Fatma, Mohamed, Madiha, Nair, Pratibha, Saif, Fatima, Tawfiq, Nafisa, Aithala, Gururaj, El-Halik, Majdi, Al-Ali, Mahmoud, Hamzeh, Abdul Rezzak

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Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa von Nair, Pratibha, Hamzeh, Abdul Rezzak, Malik, Ethar Mustafa, Oberoi, Darshjit, Al-Ali, Mahmoud Taleb, Bastaki, Fatma

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Development and validation of a questionnaire von Febin, H, Madhavan, Jithesh, Pratibha, Nair

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Quality Analysis of Manjishta (Rubia cordifolia L.) with Respect to Pharmacognostical and High-Performance Thin-Layer Chromatography Profile of the Genuine Sample: A Cross-Sectiona... von Palengara, Vivek, Harinarayanan, C. M., Nair, Pratibha P.

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Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis von Nair, Pratibha, Hamzeh, Abdul Rezzak, Mohamed, Madiha, Malik, Ethar Mustafa, Al-Ali, Mahmoud Taleb, Bastaki, Fatma

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Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders von Bizzari, Sami, Nair, Pratibha, Deepthi, Asha, Hana, Sayeeda, Al-Ali, Mahmoud Taleb, Megarbane, Andre, El-Hayek, Stephany

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Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3 von Bizzari, Sami, El-Bazzal, Lara, Nair, Pratibha, Younan, Antoine, Stora, Samantha, Mehawej, Cybel, El-Hayek, Stephany, Delague, Valerie, Mégarbané, André

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