Harpreet K. Dibra
Birmingham, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.
Journal: American journal of human genetics
Published: September 19, 2022
Childhood-Onset Movement Disorders Can Mask a Primary Immunodeficiency: 6 Cases of Classical Ataxia-Telangiectasia and Variant Forms.
Journal: Frontiers in immunology
Published: October 08, 2021
Retrospective Diagnosis of Ataxia-Telangiectasia in an Adolescent Patient With a Remote History of T-Cell Leukemia.
Journal: Journal of pediatric hematology/oncology
Published: November 20, 2019
Diagnostic Approaches to Neuroendocrine Neoplasms of Unknown Primary Site.
Journal: Neuroendocrinology
Published: September 24, 2019
Progressive epigenetic dysregulation in neuroendocrine tumour liver metastases.
Journal: Endocrine-related cancer
Published: December 17, 2016
Epigenetic dysregulation and poorer prognosis in DAXX-deficient pancreatic neuroendocrine tumours.
Journal: Endocrine-related cancer
Published: April 21, 2015
Prognostic Impact of Novel Molecular Subtypes of Small Intestinal Neuroendocrine Tumor.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: February 13, 2015
Neuroendocrine tumours: cracking the epigenetic code.
Journal: Endocrine-related cancer
Published: February 23, 2013
Showing 1-9 of 9
Last Updated: 09/26/2026