Welcome to Atlanta’s Premium Cystic Fibrosis & Bronchiectasis Service
Our mission is to create a service that works for your lifestyle. You deserve a clinic that is in tune with your needs and helps you reach your life goals. When you become a PCCA patient you gain access to a team of supportive doctors, nurses and medical assistants with your lung health as their top priority. You will have access to a host of the best physicians and surgeons in the Sandy Springs area to ensure you get the very best attention and care. Part of your personalized treatment plan may involve pulmonary rehabilitation which is delivered at Northside Hospital. Any testing which cannot be performed in the clinic can be done seamlessly at Northside Hospital across the road. We promise to get you to the best version of yourself.
Our mission is to create a service that works for your lifestyle. You deserve a clinic that is in tune with your needs and helps you reach your life goals. When you become a PCCA patient you gain access to a team of supportive doctors, nurses and medical assistants with your lung health as their top priority. You will have access to a host of the best physicians and surgeons in the Sandy Springs area to ensure you get the very best attention and care. Part of your personalized treatment plan may involve pulmonary rehabilitation which is delivered at Northside Hospital. Any testing which cannot be performed in the clinic can be done seamlessly at Northside Hospital across the road. We promise to get you to the best version of yourself.
Part of your assessment will involve genetic testing looking for rare causes of hereditary lung diseases and including mild and rare forms of cystic fibrosis.
Pulmonary function testing, lung imaging, stress tests and full physiological measurements such as cardiopulmonary exercise testing will give us all the data you need to understand your disease.
No two patients are alike. That’s why we believe in collaborating with you to create a management plan that is as unique as you.
“Seeing someone being unable to catch their breath still has a visceral effect on me. If I could help just one person feeling breathless, it would all be worth it.”
Cystic Fibrosis & Bronchiectasis Specialist
Undergraduate Education University of Edinburgh, Scotland
Medical Education University of Edinburgh, Scotland
Pulmonary Fellowship Imperial College of Medicine, London
Medical Internship Albert Einstein College of Medicine, New York
Medical Residency Albert Einstein College of Medicine, New York
Pulmonary Fellowship Emory University, Atlanta
Member of the Royal College of Physicians (Edinburgh)
Board Certified Internal Medicine
Board Certified Critical Care Medicine
Board Cerfitied Pulmonary Medicine
American College of Chest Physicians (member)
American Thoracic Society (member)
Cystic Fibrosis Foundation (fellow)
Semi-finalist in the Junior Investigators Best Abstract in Basic Science Award at the North American Cystic Fibrosis Conference
Finalist in the Adult Fellows session at the North American Cystic Fibrosis Conference
Fellows’ Teaching Award voted Best Teacher by internal medicine residents | Emory University School of Medicine
Peer Review Award for the Best Clinical Teacher | Emory University School of Medicine
Outstanding Achievement in the Teaching of Medical Students, Albert Einstein College of Medicine
Voted Best Overall House Staff at Jacobi Medical Center
Outstanding Achievement in the Teaching of Medical Students, Albert Einstein College of Medicine
Winner of Best Case Report Presentation at ACCP CHEST Meeting
Voted Best Ambulatory Care Resident at Jacobi Medical Center
Voted Best Overall House Staff at Jacobi Medical Center
Ali H. Mild Cystic Fibrosis vs. CFTR-related disorder in adulthood – That is the question! Finalist in the Adult Fellows session at the 32nd Annual North American Cystic Fibrosis Conference in Denver 2018
Ali H, Icyuz M, Kelly S, Rab A, Hong JS, Bedwell DM, Hartman IV JL, Sorscher EJ, Oliver KE. Suppression of peroxisome and ribosomal constituents partially restores plasma membrane localization and function of W1282X-CFTR. Semi-finalist in the Junior Investigators Best Abstract in Basic Science Award at the 32nd Annual North American Cystic Fibrosis Conference in Denver 2018
Ali H, Oliver KE, Icyuz M, Kelly S, Rab A, Hong JS, Bedwell DM, Hartman IV JL, Sorscher EJ. High-Throughput Yeast Phenomics Identifies Genetic Modifiers that Partially Rescue Human W1282X-CFTR. Am J Respir Crit Care Med 197; 2018: A3877
Ali H, Ajani S, Cohen L, Neujahr D, Hurtik M, Hunt WR. The effect of bone mineral density on outcomes after lung transplantation in adults with cystic fibrosis. Pediatr Pulmonol Suppl. 52; 2017: S1‐S776
Ali H, Orchard C, Mariveles M, Scott S, Bilton D, Simmonds NJ. An effective strategy for managing new and recurrent pseudomonas aeruginosa cultures in adults with cystic fibrosis. Eur Respir J. 2015 Oct;46(3): 862-5. doi:10.1183/09031936.00225914
Chang YJ, Ali H, Draper A, Chua F. An unusual cause of cyanosis in a patient with COPD. BMJ Case Rep. 2013 Mar 1;2013. pii: bcr2012008092. doi: 10.1136/bcr-2012-008092.
Fletcher TE, Ali H, Ryall C, Beeching NJ, Joekes E, Lewthwaite P. The benefits of an Infectious Disease/Radiology Multidisciplinary Team Meeting. J Infect. 2012 Oct;65(4):363-5. doi:10.1016/j.jinf.2012.05.007
Ali MH, Kalima P, Maxwell SR. Failure to implement hospital antimicrobial prescribing guidelines: a comparison of two UK academic centres. J Antimicrob Chemother. 2006 May;57(5):959-62. doi: 10.1093/jac/dkl076
Address: 960 Johnson Ferry Road, Suite 500 Atlanta GA 30342
Phone: (404) 257 0006
Timing: Monday – Friday 8:30 a.m. to 5 p.m.