Didi M[au] - Search Results

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Elective Sternotomy With Fluoroscopic Guidance for the Removal of a Residual Implantable Cardioverter Defibrillator Lead: A Case Report and Literature Review.

Khallikane S, Mehdi N, Didi M, Kbiri H, Qamouss Y. Khallikane S, et al. Among authors: didi m. Cureus. 2025 Jan 8;17(1):e77148. doi: 10.7759/cureus.77148. eCollection 2025 Jan. Cureus. 2025. PMID: 39817263 Free PMC article.

Biomarkers and Diagnostic Thresholds for Congenital Hyperinsulinism.

Petkovic G, Park J, Collingwood C, Senniappan S, Didi M. Petkovic G, et al. Among authors: didi m. Clin Endocrinol (Oxf). 2025 Feb;102(2):129-135. doi: 10.1111/cen.15137. Epub 2024 Oct 3. Clin Endocrinol (Oxf). 2025. PMID: 39360602

Bacteriological Profile of Nosocomial Pneumonia and Current State of Antibiotic Resistance in the Military Hospital of Avicenne.

Didi M, Khallikane S, Qamouss Y, Arsalane L, Zouhair S. Didi M, et al. Cureus. 2024 Aug 29;16(8):e68125. doi: 10.7759/cureus.68125. eCollection 2024 Aug. Cureus. 2024. PMID: 39347166 Free PMC article.

Variation in Glycemic Outcomes in Focal Forms of Congenital Hyperinsulinism-The UK Perspective.

Dastamani A, Yau D, Gilbert C, Morgan K, De Coppi P, Craigie RJ, Bomanji J, Biassoni L, Sajjan R, Flanagan SE, Houghton JAL, Senniappan S, Didi M, Dunne MJ, Banerjee I, Shah P. Dastamani A, et al. Among authors: didi m. J Endocr Soc. 2022 Mar 15;6(6):bvac033. doi: 10.1210/jendso/bvac033. eCollection 2022 Jun 1. J Endocr Soc. 2022. PMID: 35592516 Free PMC article.

Baseline and Peak Cortisol Response to the Low-Dose Short Synacthen Test Relates to Indication for Testing, Age, and Sex.

Park J, Titman A, Lancaster G, Selvarajah B, Collingwood C, Powell D, Das U, Dharmaraj P, Didi M, Senniappan S, Blair J. Park J, et al. Among authors: didi m. J Endocr Soc. 2022 Mar 19;6(6):bvac043. doi: 10.1210/jendso/bvac043. eCollection 2022 Jun 1. J Endocr Soc. 2022. PMID: 35506145 Free PMC article.

Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes.

Andrews A, Maharaj A, Cottrell E, Chatterjee S, Shah P, Denvir L, Dumic K, Bossowski A, Mushtaq T, Vukovic R, Didi M, Shaw N, Metherell LA, Savage MO, Storr HL. Andrews A, et al. Among authors: didi m. J Clin Endocrinol Metab. 2021 Oct 21;106(11):e4716-e4733. doi: 10.1210/clinem/dgab437. J Clin Endocrinol Metab. 2021. PMID: 34136918 Free PMC article.

Effect of Growth Hormone Therapy in Patients with Noonan Syndrome: A Retrospective Study.

Apperley LJ, Ramakrishnan R, Dharmaraj P, Das U, Didi M, Blair J, Senniappan S. Apperley LJ, et al. Among authors: didi m. Int J Endocrinol Metab. 2020 Oct 23;18(4):e107292. doi: 10.5812/ijem.107292. eCollection 2020 Oct. Int J Endocrinol Metab. 2020. PMID: 33613679 Free PMC article.

Isolated premature menarche in two siblings with Neurofibromatosis type 1.

Blackburn J, Didi M, Avula S, Senniappan S. Blackburn J, et al. Among authors: didi m. J Pediatr Endocrinol Metab. 2020 May 21;33(6):813-816. doi: 10.1515/jpem-2019-0494. J Pediatr Endocrinol Metab. 2020. PMID: 32436861

Congenital hyperinsulinism due to mutations in HNF1A.

Yau D, Colclough K, Natarajan A, Parikh R, Canham N, Didi M, Senniappan S, Banerjee I. Yau D, et al. Among authors: didi m. Eur J Med Genet. 2020 Jun;63(6):103928. doi: 10.1016/j.ejmg.2020.103928. Epub 2020 Apr 20. Eur J Med Genet. 2020. PMID: 32325224

Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution.

Brandt A, Agarwal N, Giri D, Yung Z, Didi M, Senniappan S. Brandt A, et al. Among authors: didi m. J Pediatr Endocrinol Metab. 2020 May 26;33(5):675-679. doi: 10.1515/jpem-2019-0416. J Pediatr Endocrinol Metab. 2020. PMID: 32229669

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