Currently working as Senior Professor & Head of Department of Paediatric Medicine and Incharge Rare Disease Clinic at Mahatma Gandhi Medical College and Hospital Jaipur. Currently the Executive Director of International Neonatology Association, Geneva and Chairperson Technical Committee Government of Rajasthan on Rare Diseases. Has been on the Board of the International Paediatric Association and the President of the International Society of Tropical Paediatrics. Also been on the Editorial Board of the Journal of Tropical Paediatrics- Oxford University. Press and the Advisory Board Member of the Indian Paediatrics and the Indian Journal of Practical Paediatrics. Recipient of the Fellowship from the American Academy of Paediatrics vide India Gyani Fund, Rotatory Foundation Fellowship and Neonatal visiting Fellowship from University of Illinosis of Chicago.
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Received education grant for abstract titled Hereditary fructose intolerance: unusual findings in a genotypic confirmed case in Asia Pacific digestive week (APDW 2019) at Kolkata 12-15 Dec2019.
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Oration over Epigenetics in pediatrics in Rajpedicon 2019
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Organized one day Symposium over MPS – Diagnosis and management on 11 Dec 2019.
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Invited as speaker to talk over Mucopolysacharidosis Indian perspective in 1st Asia/Middle East MPS Preceptorship Program:MPS Disease Diagnosis, Management and Treatment. 18-19 Oct 2018 Taiwan
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Poster presentation titled Hypotonia diagnostic challenges in Westneocon Nov 2019 Jaipur
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One of the team members (Dr Manisha Goyal) was facilitated by Rajasthan medical council for her work and research papers on genetics July 2017.
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Actively participated PIDCON 2018(Primary immunodeficiency diseases national conference, held on 10-11th March Jaipur.
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Faculty talk over MPS diseases in Genetic and rare diseases in Medical practice: How to recognize and manage, Feb 2018 in Jaipur
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Poster presentation in 3rd South Asia and 19th Asia LSD symposium from 20th - 22nd April 2018 in New Delhi titled Mucopolyscharidosis
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Oral presentation in 3rd South Asia and 19th Asia LSD symposium from 20th - 22nd April 2018 in New Delhi titled Skeletal manifestations in Gaucher Disease type 1
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One of the team member invited as a speaker to share experience over MPS Perspective in 1st Asia/Middle EastMPS Preceptorship Program: MPS Disease Diagnosis, Management and Treatment. 18-19 Oct 2018, Taipei Taiwan
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Poster presentation in annual conference of Indian Radiological and imaging association, at Jaipur in January 2017, titled Schmid type of Metaphyseal Chondrodysplasia: phenotype and genotype features.
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Poster presentation Cancer Genetics in 1st International conference on rare disease at Jaipur, Nov 2017
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Oral presentation in birth defect conference at New Delhi, Nov. 2016, titled ‘Lethal osteogenesis imperfect: Recurrence in an Indian family.
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Participated preconference Genetic workshop titled Genetic Disorders: Clinical and laboratory diagnosis and management on 27 Nov 2015 in 1st International conference on rare disease at Jaipur.
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Awarded second place in the poster presentation in 1st International conference on rare disease at Jaipur, Nov. 2015, titled Genotypically confirmed Stickler syndrome with unusual eye findings.
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Poster presentation in 1st International conference on rare disease at Jaipur, Nov. 2015, titled ‘Apert syndrome with preaxial polydactyly: An unusual feature.
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Invited as national speaker by government o Izrail to talk over national policy of Rare disease in Nov 2019.
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Nominated as one of the member of National policy advisory committee for Rare disease, government of India
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Chairman of National committee for National policy for treatment of Rare diseases for Rajasthan
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One of the board member of Asian alliance on Food allergy , Tokyo
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Governing board member of European academy taskforce on Food allergy
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Chairperson Rare disease taskforce Asia pacific pediatric society
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Executive director of international neonatology associations (Geneva)
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Course director food allergy, European academy Munich meetings
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Genomics of rare genetic diseases- experiences from India. Human Genomics. 2019 Sept; 25(14).
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Manisha Goyal1 & Ashok Gupta1 & Seema Kapoor2 & Anu Bhandari3 Apert Syndrome with Preaxial Polydactyly with FGFR2 Gene Mutation November 2019.
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Goyal M, Gupta A, Sharma M, Mathur P, Bansal N. Fetal Valproate Syndrome with Limb Defects: An Indian Case Report. Case Rep Pediatr. 2016;2016:3495910
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Naresh Bansal ,Ashok Gupta, Manisha Goyal, Manish Sharma, Priyanshu Mathur, Manish Agarwal. Oro Facial Digital Syndrome Type 2- An Indian case report.Journal of Pediatric Critical Care. Year : 2016 | Volume : 3 | Issue : 4 | Page : 115-117.
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Manisha Goyal, Ashok Gupta. Internet genetic resources for the clinicians. Rajasthan medical journal.
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Hypohydrotic Ectodermal Dysplasia: A rare case series. Manisha Goyal, Ashok Gupta, Priyanshu Mathur, Manish Sharma, Vol. 5 - No.1 Jan-Mar. 2018 Journal of pediatric critical care.
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Goyal M, Gupta A, Choudhary A, Bhandari A. Schmid Type Metaphyseal Chondrodysplasia with a Novel COL10A1 Mutation. Indian J Pediatr. 2018 Sep 12.
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Gupta R, Sharma P, Shukla AK, Goyal M, Gupta A. Cloacal Malformation Variant in a Male Neonate. J Indian AssocPediatr Surg. 2018 Apr-Jun;23(2):106-108.
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Rathore BS, Agnihotri A, Dube A and Gupta A. Effect of Yogic Exercises on Heart Rate Variability. Space, 2009:1, 35 – 36.
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Dube A, Gupta A, Sinha V and Deepak KK. 2010. Heart Rate Variability: A potential indicator of psycho-physiological stress. Proceedings of Theme Meeting on Advanced Applications of Physiological Variability 2010, BARC, 83 – 89.
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Dube A, Yadav K, Gupta A and Yadav Y. 2012. Neurophysiological Perspectives of electroencephalography in children with Attention Deficit Hyperactivity Disorder (ADHD). Neurophysiologie Clinique Clinical Neurophysiology, 42 (1 -2), 68.
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A rare case of compound heterozygous B-thalassemia and hereditary persistence of fetal hemoglobin with Moya-Moya disease. Ashok Gupta, Priyanshu Mathur, Manish Sharma, Vimesh Parmar . Journal of Pediatric Critical Care. 2017 Volume : 4 | Issue : 3 | Page : 110-113
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Pandit MS, Gupta A, Mathur P, Sharma M, Garg M. A case of Landau-Kleffner syndrome. J PediatrCrit Care 2016; 2: 61-63
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Gurjar M, Gupta A, Mathur P, Saroj AK. Evaluation of nutritional & educational intervention as KAP and outcome of children with SAM (6 Months - 5 years) in malnutrition treatment center. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS); Volume 15, Issue 6 Ver. III (June. 2016), PP 43-48
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Gupta V, Gupta A, Mathur P, Sharma M, Garg M. Christ-seimmens-touraine syndrome (X-linked hypohidrotic ectodermal dysplasia). Sch J Med Case Rep., 2016; 4(6): 379-381
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Pandit MS, Gupta A, Mathur P, Sharma M, Garg M, Kumar R. A case report of Kartagener syndrome. Sch J Med Case Rep., 2016; 4(6): 409-411
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Chonsariya R, Gupta A, Garg M, Mathur P, Khan K, Agarwal A. Comparison of risk factors and early morbidity in late preterm neonates and term neonates. Sch. J. App. Med. Sci., 2016; 4(8D): 2996-3001
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Gupta V, Gupta A, Mathur P, Sharma M, Garg M, Kumar R. A rare case of Wegeners granulomatosis with allergic bronchopulmonary aspergillosis in a child. J Pediatr Crit Care 2016; 3
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Kumar R Gupta A, Mathur P, Sharma M, Garg M. Extensive mongolian spots: a clinical sign merits special attention for GM1-gangliosidosis. Int J Pediatr Res.2016; 3(7): 483-486
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Garg M, Gupta A, Mathur P, Sharma M, Kumar R, Gupta V, Manjunath M. A rare case of glycogen storage disease type XI Fanconi-Bickel syndrome. J Pediatr Crit Care 2016; 3
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Kumar R, Gupta A, Mathur P, Garg M. Factor XII deficiency - A rare coagulation disorder. Indian J Child Health 2016; 12