A5019551270- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Pregnancy and preeclampsia studies
- Fetal and Pediatric Neurological Disorders
- Congenital Anomalies and Fetal Surgery
- Parvovirus B19 Infection Studies
- Pediatric Urology and Nephrology Studies
- Ectopic Pregnancy Diagnosis and Management
- Cancer Immunotherapy and Biomarkers
- Chemical and Physical Properties in Aqueous Solutions
- Pickering emulsions and particle stabilization
- Genomic variations and chromosomal abnormalities
- Crystallization and Solubility Studies
- Immunotherapy and Immune Responses
- Preterm Birth and Chorioamnionitis
- Genetic Syndromes and Imprinting
- Congenital Heart Disease Studies
- Cleft Lip and Palate Research
- Proteins in Food Systems
- Gestational Trophoblastic Disease Studies
- Congenital Diaphragmatic Hernia Studies
- vaccines and immunoinformatics approaches
- Intestinal Malrotation and Obstruction Disorders
- Congenital gastrointestinal and neural anomalies
- Pregnancy-related medical research
Indraprastha Apollo Hospitals
2015-2024
Apollo Hospitals
2013-2024
University of California, Los Angeles
2021-2023
APLA Health
2022
Apollo Cradle For Women & Children
2021
Creative Commons
2021
Rainbow Children's Hospital
2019
Metropolitan Hospital Center
2019
Commonwealth Secretariat
2010
University of Seychelles
2010
Mono-sialo-tetra-hexosylganglioside, also known as infantile GM1 gangliosidosis, is an autosomal recessive lysosomal storage disorder caused by a mutation in the GLB1 gene that stops β-galactosidase enzyme from working. We have discussed case of gangliosidosis which presented with abnormal body movements, extensive dermal melanocytosis over back and gluteal region, coarse facial features, macrocephaly. Radiological features included antero-inferior beaking second, third, fourth lumbar...
Foam separation is known to have potential for of biological molecules with a range surface activities. A statistical study (factorial design) was carried out establish the optimum operating conditions continuous foam β-casein. Maximum values enrichment β-casein into phase were found low levels initial feed protein concentration, gas flow rate, feed-flow and high heights. recovery, generally at gas-flow The highest obtained ratio 54.7 181.3, respectively, simultaneous recovery 62%; thus,...
Abstract Phase separation times for polyethylene glycol (PEG)‐4000–phosphate aqueous two‐phase systems were studied, small scale (5‐g) and large (1300‐g) systems, as a ‐function of the stability ratio. Profiles dispersion height both represented fraction initial found to be independent geometrical dimensions separator. Furthermore, by plotting time total can calculated given system at particular This generalization is important design separators. also dependent on which phases continuous. A...
ABSTRACT Sirenomelia or “mermaid syndrome” is a rare congenital abnormality with an incidence of 1 in 60,000. We report case diagnosed the first trimester using two‐dimensional, three‐dimensional, and color Doppler ultrasound. With increasing emphasis on early diagnosis fetal abnormalities, this highlights importance looking for anomalies itself. In fact, sirenomelia should be easier as severe oligohydramnios later gestation hampers vision. © 2013 Wiley Periodicals, Inc. J Clin Ultrasound 42...
Foam separation may have potential for protein recovery. However, foam to be a viable recovery technique it is important demonstrate, not only that high enrichments and recoveries can achieved single proteins, but also recoveries, together with selectivity of partition, from multi-component mixtures. Most process streams which require purification are indeed complex mixtures, example, fermentation broths. In this study, three binary mixtures were chosen continuous separation:...
To evaluate the performance of Fetal Medicine Foundation (FMF) preterm preeclampsia (PE) screening algorithm in an indigenous South Asian population.This was a prospective observational cohort study conducted tertiary maternal fetal unit Delhi, India over 2 years. The population comprised 1863 women carrying singleton pregnancy and ethnicity who were screened for pre-eclampsia between 11 14 weeks gestation using Mean Arterial Pressure (MAP), transvaginal Uterine Artery Pulsatility Index...
Anti-G has been reported as a possible cause of hemolytic disease the fetus and newborn (HDFN), either independently or in association with anti-D, anti-C both. The antibody mimics pattern anti-D reactivity identification panel is often present along both these antibodies. differentiation -C and-G routine pretransfusion workup particularly essential antenatal cases. We report two cases where anti-G was identified on advanced immunohematological workup, addition to other alloantibodies.
Abstract Background: Effective immunotherapy options are lacking for patients with advanced non-small cell lung cancer (NSCLC) who progress on a programmed death-(ligand)1 [PD-(L)1] inhibitor and those epidermal growth factor receptor (EGFR) mutation or anaplastic lymphoma kinase (ALK) rearrangement positive after progression tyrosine (TKI) therapy. One potential approach to improve immune checkpoint efficacy in these patient populations is promote cytolytic T infiltration into tumors. This...
This article highlights literacy efforts in India over the past few decades. Failure to universalize primary education, grounded as it is complex socioeconomic issues, has had serious implications for planning universal literacy. Program delivery hitherto rested with official hierarchy and included limited participation from general population. Where such did occur, programs failed due insufficient learning levels or facilities continuing education. Through use of new strategies,...
Peters' plus syndrome is a rare but clinically recognizable autosomal recessive ocular genetic syndrome. Diagnosis during the fetal life challenging due to presence of nonspecific findings such as ventriculomegaly in growth-retarded fetuses. We report first case from India, where ultrasound and family history were helpful providing clue diagnosis that was confirmed later on by DNA analysis.
Women with high-risk pregnancies are offered prenatal diagnosis through amniocentesis for cytogenetic analysis of fetal cells. The aim this study was to evaluate the effectiveness rapid fluorescence in situ hybridization (FISH) technique detecting numerical aberrations chromosomes 13, 21, 18, X and Y an Indian scenario.A total 163 samples were received a FISH and/or full karyotype from pregnancies. In 116 both conventional culture techniques getting G-banding applied conjunction test using...
Abstract Most of the fetal deformities are caused due to genetic abnormalities. Although magnetic resonance imaging (MRI) may be used accurately diagnose these deformities, it has been reported that gene analysis is a more accurate diagnostic method. Harlequin ichthyosis (HI) or Ichthyosis fetalis (IF) rare and extremely severe hereditary skin disorder with autosomal recessive inheritance. The ultrasound features have described well diagnosis can made fair degree confidence. However, final...