Mark Hannibal

Mark Hannibal

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Mark Hannibal

Mark Hannibal

Publications by authors named "Mark Hannibal"

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Altered corneal biomechanical properties in children with osteogenesis imperfecta.

J AAPOS 2018 06 7;22(3):183-187.e1. Epub 2018 Apr 7.

Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan. Electronic address:

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http://dx.doi.org/10.1016/j.jaapos.2017.12.015DOI Listing
June 2018

Hematologic Manifestations of Deficiency of Adenosine Deaminase 2 (DADA2) and Response to Tumor Necrosis Factor Inhibition in DADA2-Associated Bone Marrow Failure.

J Clin Immunol 2018 02 6;38(2):166-173. Epub 2018 Feb 6.

Pediatrics and Communicable Diseases, Pediatric Hematology/Oncology, University of Michigan, 1500 E. Medical Center Drive, D4202 Medical Professional Building, Ann Arbor, MI, 48109, USA.

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http://dx.doi.org/10.1007/s10875-018-0480-4DOI Listing
February 2018

TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections.

Cardiovasc Res 2010 Dec 13;88(3):520-9. Epub 2010 Jul 13.

Department of Internal Medicine and Cardiothoracic and Vascular Surgery, University of Texas Medical School at Houston, MSB 6.100, 6431, Fannin St, Houston, TX 77030, USA.

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http://dx.doi.org/10.1093/cvr/cvq230DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972687PMC
December 2010

The floppy infant: evaluation of hypotonia.

Pediatr Rev 2009 Sep;30(9):e66-76

Madigan Army Medical Center, Tacoma, Wash., USA.

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http://dx.doi.org/10.1542/pir.30-9-e66DOI Listing
September 2009

Clinical outcomes in lymphocytopenic lymphatic malformation patients.

Lymphat Res Biol 2007 ;5(3):169-74

Division of Pediatric Otolaryngology, Children's Hospital and Regional Medical Center, Seattle, Washington, USA.

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http://dx.doi.org/10.1089/lrb.2007.5304DOI Listing
March 2008

Aortic root dilatation is a rare complication of Noonan syndrome.

Pediatr Cardiol 2006 Jul-Aug;27(4):478-80. Epub 2006 Jul 6.

Women's & Children's Health Centre of British Columbia and Department of Pathology, Medical Genetics University of British Columbia, Vancouver, BC, Canada.

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http://dx.doi.org/10.1007/s00246-006-1210-xDOI Listing
February 2007

Lymphocytopenia in children with lymphatic malformation.

Arch Otolaryngol Head Neck Surg 2006 Jan;132(1):93-7

Department of Otolaryngology-Head and Neck Surgery, Division of Genetics and Developmental Medicine, University of Washington, Seattle, WA 98105, USA.

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http://dx.doi.org/10.1001/archotol.132.1.93DOI Listing
January 2006

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.

Am J Hum Genet 2003 Feb 27;72(2):408-18. Epub 2002 Nov 27.

Department of Pediatrics, Center for Craniofacial Development and Disorders, McKusick-Nathans Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S000292970760549
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http://dx.doi.org/10.1086/346090DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC379233PMC
February 2003

Upper limb phocomelia associated with increased nuchal translucency in a monochorionic twin pregnancy.

J Ultrasound Med 2002 Mar;21(3):355-60

Department of Medical Genetics, University of Washington Medical Center, Seattle, USA.

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http://dx.doi.org/10.7863/jum.2002.21.3.355DOI Listing
March 2002