Waldo Herrera Novey MD MBA CPE CHCQM FACP SFHM ACPAC FABQAURP (He/Him)

PubMed

• 1 citations
  Outpatient Interventions That May Enhance the Care of a Patient with Co-existing Moyamoya and Down Syndromes.
  Anita Lwanga, Waldo Herrera, Katya Y. Cruz Madrid, Antony Irungu
  Cureus. 2018-03-16

Journal Articles

• Page Kidney: A Case of Acute or Chronic Renal Failure & Refractory HTN Presenting after Renal Biopsy  
  Stephen Meyer, Aswin Nukala, Nikita Maniar*, Waldo Herrera, Open Journal of Nephrology, 2015, 5, 40-43, 6/6/2015
• Gastric leiomyoma Hospital Luis Fabrega  
  Herrera W, Rev. Med. Cient., 1/1/2004
• Severe tungiasis  
  Herrera W, Caparo I, Rev. Med. Cient., 1/1/2004
• Epidemiology and management of cardiovascular risk factors in adults 40 years of age or older Romulo Roux Health Center Pueblo Nuevo  
  Chong E, Herrera W, Rev. Med. Cient., 12/1/2002
• Type 2 diabetes mellitus: oral hypoglycemic drugs  
  Chong E, Herrera W, Rev. Med. Cient., 12/1/2002
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Abstracts/Posters

• An atypical case of moyamoya syndrome.
  Lwanga A, Herrera W, Cruz K, Irungu A., Journal of the American Geriatrics Society. Volume66, IssueS2, April 2018, Pages S1-S369., 4/2018
• Sacral osteomyelitis in Crohn's disease.
  Herrera W, Baru J, Mechurova J, 7th Annual Midwestern Hospital Medicine Conference, Chicago, IL, 9/1/2011
• Sacral osteomyelitis in Crohn's disease.
  Herrera W, Mechurova J, Baru J, Department of Medicine, 6th Annual Resident Research and Poster Day, Chicago, IL, 4/1/2010
• Pylethrombosis of the portal vein.
  Herrera W, Mechurova J, Department of Medicine, 6th Annual Resident Research and Poster Day, Chicago, IL, 4/1/2010
• Amyloid cardiomyopathy.
  Mechurova J, Herrera W, Pandey T, Department of Medicine, 6th Annual Resident Research and Poster Day, Chicago, IL, 4/1/2010
• Acute hemorrhagic leukoencephalitis.
  Herrera W, Department of Medicine, 6th Annual Resident Research and Poster Day, Chicago, IL, 4/1/2010
• CERKL mutations cause retina-wide rod and cone disease with prominent maculopathy.
  Aleman TS, Cideciyan AV, Sumaroka AM, Windsor EAM, Russell RC, Herrera W, Roman AJ, Schwartz SB, Fishman GA, Jacobson SG, Invest Ophthalmol Vis Sci, 1/1/2009
• Retinal disease caused by USH2A mutations.
  Aleman TS, Cideciyan AV, Roman AJ, Sumaroka A, Schwartz SB, Herrera W, Windsor EAM, Stone EM, Liu XZ, Jacobson SG, Invest Ophthalmol Vis Sci, 5/1/2008
• Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.
  Herrera W, Aleman TS, Cideciyan AV, Roman AJ, Banin E, Ben-Yosef T, Gardner LM, Sumaroka A, Kimberling WJ, Jacobson SG, Invest Ophthalmol Vis Sci, 5/1/2008
• The investigation of transcapillary filtration changes in patients with venous insufficiency and undergoing surgery for varicose veins.
  Aslam M, Parmer J, Shawish E, Misurati T, Herrera W, Sehlawi M, Ryan CJ, Standfield N, Int Angiol, 6/1/2006
• A comparative study of three noninvasive techniques to detect peripheral arterial occlusive disease.
  Herrera W, Aslam M, Misurati T, Shawish E, Standfield N, Int Angiol, 6/1/2006
• New scoring system for carotid stenosis based on duplex ultrasound and clinical parameters.
  Shawish E, Aslam M, Misurati T, Herrera W, Humphries K, Standfield N, Int Angiol, 6/1/2006
• The evaluation of a novel noninvasive, passive optical device as a reliable screening tool for patients with suspicion of deep vein thrombosis.
  Misurati T, Aslam M, Evans J, Gough N, Shawish E, Herrera W, Standfield N, Int Angiol, 1/1/2006
• CERKL mutations cause retina-wide rod and cone disease with prominent maculopathy.
  Aleman TS, Cideciyan AV, Sumaroka AM, Windsor EAM, Russell RC, Herrera W, Roman AJ, Schwartz SB, Fishman GA, Jacobson SG, Association for Research in Vision and Ophthalmology 2009 Annual Meeting, Fort Lauderdale, FL
• Retinal disease caused by USH2A mutations.
  Aleman TS, Cideciyan AV, Roman AJ, Sumaroka A, Schwartz SB, Herrera W, Windsor EAM, Stone EM, Liu XZ, Jacobson SG, Association for Research in Vision and Ophthalmology 2008 Annual Meeting, Fort Lauderdale, FL
• Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.
  Herrera W, Aleman TS, Cideciyan AV, Roman AJ, Banin E, Ben-Yosef T, Gardner LM, Sumaroka A, Kimberling WJ, Jacobson SG, Association for Research in Vision and Ophthalmology 2008 Annual Meeting, Fort Lauderdale, FL
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Lectures

• A comparative study of three noninvasive techniques to detect peripheral arterial occlusive disease. 
  Lisbon, Portugal - 6/1/2006