» Authors » S Shahrukh Hashmi

S Shahrukh Hashmi

Explore the profile of S Shahrukh Hashmi including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 60
Citations 666
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
11.
Maili L, Ruiz O, Kahan P, Chiu F, Larson S, Hashmi S, et al.
Dis Model Mech . 2023 Apr; 16(6). PMID: 37102214
Facial development requires a complex and coordinated series of cellular events that, when perturbed, can lead to structural birth defects. A quantitative approach to quickly assess morphological changes could address...
12.
Brar B, Bober M, Gough E, Hashmi S, Hecht J, Dujmusic L, et al.
Genet Med . 2023 Apr; 25(7):100845. PMID: 37061874
Purpose: Pregnancies affected by maternal or fetal achondroplasia present unique challenges. The optimal route of delivery in fetuses with achondroplasia has not been established. Our objective was to determine whether...
13.
Gibson A, Montanez N, Addy K, Hashmi S, Brown D, Rodriguez N, et al.
J Pediatr Hematol Oncol . 2022 Nov; 45(5):e655-e659. PMID: 36449733
Introduction: Once-daily enoxaparin (ODE), considered standard of care for venous thromboembolism (VTE) treatment in adults, has been infrequently assessed in children. To contribute available data to a limited field, we...
14.
Johnson A, Bannon S, Farach L, Hyde S, Hashmi S, Wagner C, et al.
Eur J Haematol . 2022 Oct; 110(1):109-116. PMID: 36209474
Since 2003, more than 15 genes have been identified to predispose to hereditary hematologic malignancy (HHM). Although the yield of germline analysis for leukemia appears like that of solid tumors,...
15.
Hoover-Fong J, Schulze K, Alade A, Bober M, Gough E, Hashmi S, et al.
Orphanet J Rare Dis . 2021 Dec; 16(1):522. PMID: 34949201
Background: Achondroplasia is the most common genetic skeletal disorder causing disproportionate short stature/dwarfism. Common additional features include spinal stenosis, midface retrusion, macrocephaly and a generalized spondylometaphyseal dysplasia which manifest as...
16.
Tunkel D, Gough E, Bober M, Hashmi S, Hecht J, Legare J, et al.
Laryngoscope . 2021 Oct; 132(8):1548-1554. PMID: 34708868
Objectives/hypothesis: To quantify otolaryngologic surgery utilization in patients with achondroplasia, and to identify any changes in utilization over the past four decades. Study Design: Retrospective cohort study. Methods: A retrospective...
17.
Legare J, Liu C, Pauli R, Alade A, Hashmi S, Campbell J, et al.
J Neurosurg Pediatr . 2021 Jun; 28(2):229-235. PMID: 34087800
Objective: The authors sought to determine the overall incidence of cervicomedullary decompression (CMD) in patients with achondroplasia and the characteristics associated with those surgeries across multiple institutions with experience caring...
18.
Hoover-Fong J, Alade A, Hashmi S, Hecht J, Legare J, Little M, et al.
Genet Med . 2021 May; 23(8):1498-1505. PMID: 34006999
Purpose: Achondroplasia is the most common short stature skeletal dysplasia (1:20,000-30,000), but the risk of adverse health outcomes from cardiovascular diseases, pain, poor function, excess weight, and sleep apnea is...
19.
Koutroumpakis E, Hashmi S, Powell C, Fatakdawala M, Pang J, Patel R, et al.
Cardiology . 2021 Apr; 146(4):481-488. PMID: 33902039
Introduction: Cardiovascular comorbidities may predispose to adverse outcomes in hospitalized patients with coronavirus disease 2019 (COVID-19). However, across the USA, the burden of cardiovascular comorbidities varies significantly. Whether clinical outcomes...
20.
Mowrey K, Northrup H, Rougeau P, Hashmi S, Krueger D, Ebrahimi-Fakhari D, et al.
Front Neurol . 2021 Apr; 12:627672. PMID: 33897589
Tuberous sclerosis complex (TSC) is a genetic condition that causes benign tumors to grow in multiple organ systems. Nonfunctional pancreatic neuroendocrine tumors (PNETs) are a rare clinical feature of TSC...