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Sujatha Jagadeesh

Showing results (1-10 of 38) with videos related to

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Indian Pediatrics|August 5, 2011
Cartilage-hair hypoplasia caused by novel compound heterozygous RMRP mutationsKerstin Reicherter, Amithkumar Iynapillai Veeramani, Sujatha Jagadeesh
Indian Pediatrics|November 14, 2013
Citrullinemia type 1: genetic diagnosis and prenatal diagnosis in subsequent pregnancyG Karthikeyan, Sujatha Jagadeesh, Suresh Seshadri, et al.
The National Medical Journal of India|September 27, 2013
Biotinidase deficiency: an atypical presentationSujatha Jagadeesh, Beena Suresh, Suresh Seshadri, et al.
Ocular Immunology and Inflammation|October 15, 2024
Uveal Effusion Syndrome Due to WNT10A MutationGazal Patnaik, Sujatha Jagadeesh, Muna Bhende, et al.
Neuro-Ophthalmology (Aeolus Press)|November 20, 2019
A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)Beena Suresh, Vaishnavi Reddy, Ingo Kurth, et al.
Indian Journal of Pediatrics|February 18, 2011
Fanconi-Bickel syndromeMohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, et al.
Indian Pediatrics|April 23, 2009
Prenatal diagnosis of restrictive dermopathySujatha Jagadeesh, Lathaa Bhat, Indrani Suresh, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 30, 2016
Usefulness of fetal autopsy in the diagnosis of blomstrand chondrodysplasia: a report of three casesSuresh Beena, Lata Murlidhar, Suresh Seshadri, et al.
Prenatal Diagnosis|January 21, 2003
Second trimester diagnosis of Neu Laxova syndromeM A Shivarajan, S Suresh, Sujatha Jagadeesh, et al.
BMJ Case Reports|January 28, 2025
Central congenital hypothyroidism due to TSHB gene mutation: 25-year follow-upAdlyne Reena Asirvatham, Vaishnavi Reddy Deva Reddy, Sujatha Jagadeesh, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Indian Pediatrics|August 5, 2011
Cartilage-hair hypoplasia caused by novel compound heterozygous RMRP mutationsKerstin Reicherter, Amithkumar Iynapillai Veeramani, Sujatha Jagadeesh
Indian Pediatrics|November 14, 2013
Citrullinemia type 1: genetic diagnosis and prenatal diagnosis in subsequent pregnancyG Karthikeyan, Sujatha Jagadeesh, Suresh Seshadri, et al.
The National Medical Journal of India|September 27, 2013
Biotinidase deficiency: an atypical presentationSujatha Jagadeesh, Beena Suresh, Suresh Seshadri, et al.
Ocular Immunology and Inflammation|October 15, 2024
Uveal Effusion Syndrome Due to WNT10A MutationGazal Patnaik, Sujatha Jagadeesh, Muna Bhende, et al.
Neuro-Ophthalmology (Aeolus Press)|November 20, 2019
A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)Beena Suresh, Vaishnavi Reddy, Ingo Kurth, et al.
Indian Journal of Pediatrics|February 18, 2011
Fanconi-Bickel syndromeMohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, et al.
Indian Pediatrics|April 23, 2009
Prenatal diagnosis of restrictive dermopathySujatha Jagadeesh, Lathaa Bhat, Indrani Suresh, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 30, 2016
Usefulness of fetal autopsy in the diagnosis of blomstrand chondrodysplasia: a report of three casesSuresh Beena, Lata Murlidhar, Suresh Seshadri, et al.
Prenatal Diagnosis|January 21, 2003
Second trimester diagnosis of Neu Laxova syndromeM A Shivarajan, S Suresh, Sujatha Jagadeesh, et al.
BMJ Case Reports|January 28, 2025
Central congenital hypothyroidism due to TSHB gene mutation: 25-year follow-upAdlyne Reena Asirvatham, Vaishnavi Reddy Deva Reddy, Sujatha Jagadeesh, et al.
Pageof 4