Publications by authors named "Veronica Arora"

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Unusual Dual Fungal Infection in STAT1 Gain-of-Function CMC: Clinical and Mycological Insights.
Tanvi Dev, Veronica Arora, Protick Kumar Mondal, Vishal Gaurav, Aditi Guglani

Int J Dermatol· January 2026

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-Related Beckwith-Wiedemann Syndrome: First Patient from India.
Veronica Arora, Aashita Takkar, Sudhisha Dubey, Deepti Gupta, Renu Saxena

J Pediatr Genet· December 2024

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The molecular landscape of oculocutaneous albinism in India and its therapeutic implications.
Sudha Kohli, Renu Saxena, Ratna Dua Puri, Sunita Bijarnia Mahay, Swasti Pal, Veronica Arora

Eur J Hum Genet· October 2024

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A Further Case of Larsen's Syndrome: Clinical and Genotypic Challenges in Diagnosis.
Veronica Arora, Swasti Pal, Samarth Kulshreshtha, Ishwar C Verma

J Pediatr Genet· December 2022

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Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene.
Aashita Takkar, Veronica Arora, Renu Saxena, Praveen Kumar, I C Verma

Indian J Pediatr· November 2022

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Fragile X Syndrome Due to a Frameshift Deletion: A Rare Mechanism.
Veronica Arora, Aashita Takkar, Ashima Mehta, Neerja Malleda, Praveen Kumar

Indian J Pediatr· September 2022

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Clinical Remission of Immunoglobulin A Nephropathy after Bariatric Surgery in a Young Morbidly Obese Patient.
Vaibhav Tiwari, Anurag Gupta, Veronica Arora, Pallav Gupta, Suviraj John

Saudi J Kidney Dis Transpl· August 2022

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COMMENT: The Medical Termination of Pregnancy (Amendment) Act, 2021: A step towards liberation.
Veronica Arora, Ishwar C Verma

Indian J Med Ethics· June 2022

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Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up.
Aakriti Kapoor, Tushar Kapoor, Aakaar Kapoor, Apurva Kapoor, Ravi Kapoor, Veronica Arora

J Clin Imaging Sci· May 2022

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Osteopathia Striata with Cranial Sclerosis: A Face-to-Radiograph-to-Gene Diagnosis.
Veronica Arora, Sunita Bijarnia-Mahay, K K Saxena, Praveen Suman, Shyam Kukreja

J Pediatr Genet· March 2022

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Risk factors for Coronavirus disease-associated mucormycosis.
Umang Arora, Megha Priyadarshi, Varidh Katiyar, Manish Soneja, Prerna Garg, Veronica Arora

J Infect· March 2022

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Implications of a Genetic Etiology for Renal Transplant: Early-Onset Alport Syndrome with a Novel Mutation.
Ravi Kumar Singh, Veronica Arora, Vaibhav Tiwari, Deepti Gupta, Anurag Gupta

J Pediatr Genet· December 2021

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Hypervitaminosis D and Acute Interstitial Nephritis: Tale of Injections.
Vaibhav Tiwari, Veronica Arora, Jitendra Rajput, Anurag Gupta, Smita Divyaveer

Indian J Nephrol· December 2021

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Genetic Testing in Pediatric Epilepsy.
Ishwar C Verma, Sameer Bhatia, Veronica Arora

Indian J Pediatr· October 2021

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Neuro-Regression in a Child with Silvery Hair.
Veronica Arora, Monika Jain, Ishwar C Verma

Indian J Pediatr· June 2021

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Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss.
Meenakshi Lallar, Veronica Arora, Renu Saxena, Ratna Dua Puri, Ishwar Chander Verma

J Pediatr Genet· March 2021

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Hypophosphatemic Rickets with R179W Mutation in FGFR23 Gene - A Rare But Treatable Cause of Refractory Rickets.
Sapna Sandal, Veronica Arora, Ishwar C Verma

Indian J Pediatr· January 2021

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ANO5-associated Gnathodiaphyseal dysplasia with calvarial doughnut lesions: First report in an Asian Indian with an expanded phenotype.
Sapna Sandal, Veronica Arora, Ishwar C Verma

Congenit Anom (Kyoto)· January 2021

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Biallelic Pathogenic Variants Cause Autosomal Recessive Bilateral Renal Agenesis.
Veronica Arora, Suliman Khan, Ayman W El-Hattab, Ratna Dua Puri, Maria Eugenia Rocha

J Am Soc Nephrol· January 2021

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Eyes See what the Mind Knows: Clues to Pattern Recognition in Single Enzyme Deficiency-Related Peroxisomal Disorders.
Veronica Arora, Sunita Bijarnia-Mahay, Sudhisha Dubey, Renu Saxena

Mol Syndromol· December 2020

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Genetic Testing in Pediatric Kidney Disease.
Veronica Arora, Kanav Anand, Ishwar Chander Verma

Indian J Pediatr· September 2020

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Unique skeletal manifestations in patients with Primrose syndrome.
Veronica Arora, Eyby Leon, Jullianne Diaz, Hanne Buciek Hove, Daniel Rocha Carvalho

Eur J Med Genet· August 2020

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A further case of hypotonia, ataxia, developmental delay and tooth enamel defect syndrome due to a recurrent C-terminal binding protein 1 mutation.
Sameer Kumar Bhatia, Veronica Arora, Ishwar Chander Verma

Clin Dysmorphol· July 2020

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Expanding the phenotypic and genotypic spectrum of Wiedemann-Steiner syndrome: First patient from India.
Veronica Arora, Ratna D Puri, Sunita Bijarnia-Mahay, Ishwar C Verma

Am J Med Genet A· May 2020

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