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Stereomicroscopic analysis of microleakage, evaluation of shear bond strengths and adhesive remnants beneath orthodontic brackets under cyclic exposure to commonly consumed commercial "soft" drinks

Indian journal of dental research, 2021-01, Vol.32 (1), p.98-103

2021

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The perception of attractiveness of the facial profile among people of Telangana ethnicity

Journal of Dr. NTR university of health sciences, 2022-07, Vol.11 (3), p.193-199

2022

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CHARGE syndrome

Orphanet journal of rare diseases, 2006-09, Vol.1 (1), p.34-34, Article 34

2006

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Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report

Frontiers in neurology, 2024-02, Vol.15, p.1204848

2024

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Alleviation of Lower Anterior Crowding with Super- Elastic and Heat-Activated NiTi Wires: A Prospective Clinical Trial

Turkish Journal of Orthodontics, 2021-06, Vol.34 (2), p.127-135

2021

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A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report

Frontiers in neurology, 2023-09, Vol.14

2023

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An Unexpected Finding of Hepatosplenomegaly in a Pediatric Patient

Clinical pediatrics, 2022-01, Vol.61 (1), p.81-85

2022

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Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease: Case and Review

Canadian journal of neurological sciences, 2019-07, Vol.46 (4), p.459-463

2019

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Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario

Journal of human genetics, 2021-05, Vol.66 (5), p.451-464

2021

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Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report

Frontiers in neurology, 2023-10, Vol.14

2023

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De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures

Frontiers in neurology, 2021-12, Vol.12, p.804078-804078

2021

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Bolton's analysis using a photogrammetric method on occlusal photographs

European oral research, 2020-05, Vol.54 (2), p.55-61

2020

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Pyruvate dehydrogenase deficiency and epilepsy

Brain & development (Tokyo. 1979), 2011-11, Vol.33 (10), p.856-865

2011

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In vivo investigation of gingival health and oxidative stress changes in patients undergoing orthodontic treatment with and without fluoride use

Journal of Indian Society of Periodontology, 2022-03, Vol.26 (2), p.123-129

2022

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Perceptions of facial proportions and lip competency on facial attractiveness among people of Telangana origin

Journal of Dr. NTR university of health sciences, 2019-07, Vol.8 (3), p.183-191

2019

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Methylmalonic aciduria as a biochemical marker for mitochondrial DNA depletion syndrome in patients with developmental delay and movement disorders: a case series

Frontiers in neurology, 2023, Vol.14, p.1265115-1265115

2023

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Methylenetetrahydrofolate reductase (MTHFR) deficiency and infantile epilepsy

Brain & development (Tokyo. 1979), 2011-10, Vol.33 (9), p.758-769

2011

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Menkes disease and infantile epilepsy

Brain & development (Tokyo. 1979), 2011-11, Vol.33 (10), p.866-876

2011

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Pitfalls in Genetic Testing for Consanguineous Pediatric Populations

Case reports in genetics, 2022-05, Vol.2022, p.9393042-3

2022

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Benign reactive lymphadenopathy associated with submandibular gland enlargement during orthodontic treatment

Journal of oral and maxillofacial pathology : JOMFP, 2017-01, Vol.21 (1), p.181-182

2017

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Parental psychosocial aspects and stressors involved in the management of inborn errors of metabolism

Molecular genetics and metabolism reports, 2020-12, Vol.25, p.100654-100654, Article 100654

2020

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Evaluating upper lip changes during smiling and at rest in Indian population

Indian journal of dental research, 2021-04, Vol.32 (2), p.167-173

2021

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Road to a rare diagnosis: Description of novel unbalanced translocation causing partial trisomy 17p

Clinical case reports, 2022-10, Vol.10 (10), p.n/a

2022

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Deletion of 15q11.2(BP1-BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population

American journal of medical genetics. Part A, 2015-09, Vol.167A (9), p.2098-2102

2015

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Dual diagnosis of trisomy 21 and lethal perinatal Gaucher disease as a cause of non‐immune hydrops fetalis in a twin pregnancy for a consanguineous couple

Clinical case reports, 2023-08, Vol.11 (8), p.n/a

2023

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Stereomicroscopic analysis of microleakage, evaluation of shear bond strengths and adhesive remnants beneath orthodontic brackets under cyclic exposure to commonly consumed commercial "soft" drinks

The perception of attractiveness of the facial profile among people of Telangana ethnicity

CHARGE syndrome

Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report

Alleviation of Lower Anterior Crowding with Super- Elastic and Heat-Activated NiTi Wires: A Prospective Clinical Trial

A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report

An Unexpected Finding of Hepatosplenomegaly in a Pediatric Patient

Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease: Case and Review

Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario

Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report

De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures

Bolton's analysis using a photogrammetric method on occlusal photographs

Pyruvate dehydrogenase deficiency and epilepsy

In vivo investigation of gingival health and oxidative stress changes in patients undergoing orthodontic treatment with and without fluoride use

Perceptions of facial proportions and lip competency on facial attractiveness among people of Telangana origin

Methylmalonic aciduria as a biochemical marker for mitochondrial DNA depletion syndrome in patients with developmental delay and movement disorders: a case series

Methylenetetrahydrofolate reductase (MTHFR) deficiency and infantile epilepsy

Menkes disease and infantile epilepsy

Pitfalls in Genetic Testing for Consanguineous Pediatric Populations

Benign reactive lymphadenopathy associated with submandibular gland enlargement during orthodontic treatment

Parental psychosocial aspects and stressors involved in the management of inborn errors of metabolism

Evaluating upper lip changes during smiling and at rest in Indian population

Road to a rare diagnosis: Description of novel unbalanced translocation causing partial trisomy 17p

Deletion of 15q11.2(BP1-BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population

Dual diagnosis of trisomy 21 and lethal perinatal Gaucher disease as a cause of non‐immune hydrops fetalis in a twin pregnancy for a consanguineous couple

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