[HTML][HTML] Epigenetics in Kawasaki disease
Kawasaki disease (KD) is a common febrile multisystemic inflammatory illness in children
that preferentially affects coronary arteries. Children with KD who develop coronary artery …
that preferentially affects coronary arteries. Children with KD who develop coronary artery …
[PDF][PDF] Complaint management-review and additional insights
Research on complaint management has been substantially growing over the last few years.
Firms have started to realize the importance of complaint management as defensive …
Firms have started to realize the importance of complaint management as defensive …
Impact of the internet on teenagers' influence on family purchases
A Kaur, Y Medury - Young Consumers, 2011 - emerald.com
Based on a survey administered to 346 parent‐child dyads, regression analysis and ANOVA
analysis were employed to analyze the impact of the internet on teenagers' influence on …
analysis were employed to analyze the impact of the internet on teenagers' influence on …
Destination image of Indian tourism destinations: An evaluation using correspondence analysis
A Kaur, A Chauhan, Y Medury - Asia Pacific Journal of Marketing and …, 2016 - emerald.com
Purpose–The purpose of this paper is to evaluate tourist destinations' image based on the
attributes obtained from the extant literature using correspondence analysis …
attributes obtained from the extant literature using correspondence analysis …
Current role of genetics in hematologic malignancies
Rapidly changing field of genetic technology and its application in the management of
hematological malignancies has brought significant improvement in treatment and outcome …
hematological malignancies has brought significant improvement in treatment and outcome …
Clinical and molecular features of 66 patients with musculocontractural Ehlers− Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
M Minatogawa, A Unzaki, H Morisaki, D Syx… - Journal of medical …, 2022 - jmg.bmj.com
Background Musculocontractural Ehlers− Danlos syndrome is caused by biallelic loss-of-
function variants in CHST14 (mcEDS-CHST14) or DSE (mcEDS-DSE). Although 48 patients …
function variants in CHST14 (mcEDS-CHST14) or DSE (mcEDS-DSE). Although 48 patients …
[HTML][HTML] Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation
J Sheth, R Bhavsar, M Mistri, D Pancholi… - BMC medical …, 2019 - Springer
Background Gaucher disease is a rare pan-ethnic, lysosomal storage disorder resulting due
to beta-Glucosidase (GBA1) gene defect. This leads to the glucocerebrosidase enzyme …
to beta-Glucosidase (GBA1) gene defect. This leads to the glucocerebrosidase enzyme …
Long-term epilepsy control, motor function, cognition, sleep and quality of life in children with West syndrome
S Bhanudeep, P Madaan, N Sankhyan, L Saini… - Epilepsy Research, 2021 - Elsevier
Purpose To assess epilepsy, motor function, cognitive, sleep, and quality of life outcomes
and their predictors in a follow-up cohort with West syndrome (WS) at≥ 5 years of age …
and their predictors in a follow-up cohort with West syndrome (WS) at≥ 5 years of age …
[PDF][PDF] Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism
ANKRD17 is an ankyrin repeat-containing protein thought to play a role in cell cycle
progression, whose ortholog in Drosophila functions in the Hippo pathway as a co-factor of …
progression, whose ortholog in Drosophila functions in the Hippo pathway as a co-factor of …
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities
P Kaur, MC do Rosario, M Hebbar, S Sharma… - Clinical …, 2021 - Wiley Online Library
Genetic disorders with predominant central nervous system white matter abnormalities (CNS
WMAs), also called leukodystrophies, are heterogeneous entities. We ascertained 117 …
WMAs), also called leukodystrophies, are heterogeneous entities. We ascertained 117 …