Cargando…

The association of dyslipidemia and obesity with glycated hemoglobin

BACKGROUND: Dyslipidemia and obesity are the most common complex metabolic disorders taking the highest toll of health resources globally by its increasing incidences. This consequently leads to type 2 diabetes mellitus (T2DM) and cardiovascular disorders (CVDs) with variable reports about the role...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sheth, Jayesh, Shah, Ankna, Sheth, Frenny, Trivedi, Sunil, Nabar, Nutan, Shah, Navneet, Thakor, Premal, Vaidya, Rama
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469195/ https://www.ncbi.nlm.nih.gov/pubmed/28702225 http://dx.doi.org/10.1186/s40842-015-0004-6

Ejemplares similares

Does vitamin D play a significant role in type 2 diabetes?
por: Sheth, Jayesh J, et al.
Publicado: (2015)

Effect of PPAR-γ2 gene Pro12Ala and ADR-β3 gene Trp64AArg polymorphism on glucose homeostasis in Type 2 diabetes subjects from Western India
por: Shah, Ankna, et al.
Publicado: (2014)

Association of Vitamin D(3) levels with glycemic control in Type 2 diabetes subjects from Gujarati population-India
por: Majumder, Avisek, et al.
Publicado: (2014)

Effect of PPAR-γ2 Gene Pro12Ala polymorphism (Rs1801282) and Vitamin D(3) on glucose homeostasis in Type 2 diabetic subjects from Gujarat-India
por: Majumder, Avisek, et al.
Publicado: (2014)

The GALNS p.P77R variant is a probable Gujarati-Indian founder mutation causing Mucopolysaccharidosis IVA syndrome
por: Sheth, Harsh, et al.
Publicado: (2022)

Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children – a case report with a review
por: Sheth, Jayesh, et al.
Publicado: (2019)

A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature
por: Sheth, Frenny, et al.
Publicado: (2018)

Pure interstitial dup(6)(q22.31q22.31) – a case report
por: Sheth, Frenny, et al.
Publicado: (2015)

Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation
por: Sheth, Frenny, et al.
Publicado: (2015)

Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report
por: Sheth, Harsh, et al.
Publicado: (2020)

Glycative Stress, Glycated Hemoglobin, and Atherogenic Dyslipidemia in Patients with Hyperlipidemia
por: Yao, Chien-An, et al.
Publicado: (2023)

Case Report: Recurrent Variant c.298 TA in CCN6 Gene Found in Progressive Pseudorheumatoid Dysplasia Patients From Patni Community of Gujarat: A Report of Three Cases
por: Sheth, Harsh, et al.
Publicado: (2021)

A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report
por: Sheth, Frenny, et al.
Publicado: (2023)

GM2 gangliosidosis AB variant: novel mutation from India – a case report with a review
por: Sheth, Jayesh, et al.
Publicado: (2016)

Prenatal screening of cytogenetic anomalies – a Western Indian experience
por: Sheth, Frenny, et al.
Publicado: (2015)

Pulmonary manifestations in Niemann-Pick type C disease with mutations in NPC2 gene: case report and review of literature
por: Sheth, Jayesh, et al.
Publicado: (2017)

Late infantile and adult‐onset metachromatic leukodystrophy due to novel missense variants in the PSAP gene: Case report from India
por: Sheth, Jayesh, et al.
Publicado: (2023)

Prenatal diagnosis of Tay-Sachs disease: our institutional experience
por: Sheth, Jayesh, et al.
Publicado: (2014)

Prenatal diagnosis of lysosomal storage disorders: our experience in 120 cases
por: Mistri, Mehul, et al.
Publicado: (2014)

Late infantile form of multiple sulfatase deficiency with a novel missense variant in the SUMF1 gene: case report and review
por: Sheth, Jayesh, et al.
Publicado: (2023)

Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15
por: Tewari, Stuti, et al.
Publicado: (2017)

An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene: a case report
por: Bajaj, Shruti, et al.
Publicado: (2022)

Identification of novel mutations in HEXA gene in children affected with Tay-Sachs disease from India
por: Mistri, Mehul, et al.
Publicado: (2014)

Frequency analysis of Spinocerebellar ataxia types 1, 2, 3 & 6 in patients with ataxia from Gujarat
por: Patel, Harsh, et al.
Publicado: (2014)

A case of Raine syndrome presenting with facial dysmorphy and review of literature
por: Sheth, Jayesh, et al.
Publicado: (2018)

Identification of Novel Mutations in FAH Gene and Prenatal Diagnosis of Tyrosinemia in Indian Family
por: Sheth, Jayesh J., et al.
Publicado: (2012)

A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome
por: Shah, Jhanvi, et al.
Publicado: (2021)

Characterization of prenatally detected small Supernumerary Marker Chromosomes (sSMC) by molecular cytogenetic technique: FISH
por: Patel, Bhumi, et al.
Publicado: (2014)

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report
por: Mistri, Mehul, et al.
Publicado: (2014)

Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study
por: Sheth, Frenny J, et al.
Publicado: (2013)

Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease
por: Sheth, Jayesh, et al.
Publicado: (2014)

Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter
por: Sheth, Frenny, et al.
Publicado: (2013)

Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome
por: Sheth, Frenny, et al.
Publicado: (2012)

Identification of novel mutations in glucocerebrosidase (GBA) gene in Indian patients with gaucher disease (GD)
por: Ankleshwaria, Chitra, et al.
Publicado: (2014)

Diagnostic utility of array-based Comparative Genomic Hybridization in a clinical setting
por: Sheth, Frenny, et al.
Publicado: (2014)

Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India
por: Sheth, Jayesh, et al.
Publicado: (2018)

Detection and Inheritance Pattern of Copy Number Variations (CNVs) in Children with Multiple Congenital Anomalies
por: Sheth, Frenny
Publicado: (2014)

Partial deletion of distal long arm encompassing Jacobsen Syndrome
por: Desai, Manisha, et al.
Publicado: (2014)

Distal Deletion of Chromosome 11q Encompassing Jacobsen Syndrome without Platelet Abnormality
por: Sheth, Frenny J, et al.
Publicado: (2014)

Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in India
por: Sheth, Jayesh, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_0jnmubjuvvtjbp3ofqjtm860c5