Works matching Peyton Manning

Results: 77

Athletes' Use of Unproven Stem Cell Therapies: Adding to Inappropriate Media Hype?

Published in:

Molecular Therapy, 2012, v. 20, n. 9, p. 1656, doi. 10.1038/mt.2012.172

By:

Caulfield, Timothy;
McGuire, Amy

Publication type:

Article

PLAY BALL!

Published in:

2008

By:

Howard, Sara Catherine

Publication type:

Book Review

Concerning the Effect of Athlete Endorsements on Brand and Team-Related Intentions.

Published in:

Sport Marketing Quarterly, 2008, v. 17, n. 3, p. 154

By:

Carison, Brad D.;
Donavan, D. Todd

Publication type:

Article

More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome.

Published in:

Human Mutation, 2021, v. 42, n. 6, p. 711, doi. 10.1002/humu.24199

By:

Dhooge, Tibbe;
Van Damme, Tim;
Syx, Delfien;
Mosquera, Laura M.;
Nampoothiri, Sheela;
Radhakrishnan, Anil;
Simsek‐Kiper, Pelin O.;
Utine, Gülen E.;
Bonduelle, Maryse;
Migeotte, Isabelle;
Essawi, Osama;
Ceylaner, Serdar;
Al Kindy, Adila;
Tinkle, Brad;
Symoens, Sofie;
Malfait, Fransiska

Publication type:

Article

Palliative Care for Children with Central Nervous System Malignancies.

Published in:

Bioengineering (Basel), 2018, v. 5, n. 4, p. 1, doi. 10.3390/bioengineering5040085

By:

Baenziger, Peter H.;
Moody, Karen

Publication type:

Article

Cardiotoxicity of CPX-351 in children and adolescents with relapsed AML: a Children's Oncology Group report.

Published in:

Frontiers in Cardiovascular Medicine, 2024, p. 1, doi. 10.3389/fcvm.2024.1347547

By:

Leger, Kasey J.;
Absalon, Michael J.;
Demissei, Biniyam G.;
Smith, Amanda M.;
Gerbing, Robert B.;
Alonzo, Todd A.;
Narayan, Hari K.;
Hirsch, Betsy A.;
Pollard, Jessica A.;
Razzouk, Bassem I.;
Getz, Kelly D.;
Aplenc, Richard;
Kolb, E. Anders;
Ky, Bonnie;
Cooper, Todd M.

Publication type:

Article

Pineal gland hypermetabolic involvement without central nervous system symptoms in a pediatric patient with primary nodular sclerosis subtype classical Hodgkin Lymphoma.

Published in:

2022

By:

Kokoska, Ryan E.;
Beltz, Eric E.;
Smith, Jodi L.;
Razzouk, Bassem I.

Publication type:

Report

Indications for cerebral revascularization for moyamoya syndrome in pediatric sickle cell disease determined by Delphi methodology.

Published in:

Journal of Neurosurgery: Pediatrics, 2024, v. 34, n. 4, p. 402, doi. 10.3171/2024.5.PEDS2426

By:

Robert, Adam P.;
Hanel, Ricardo A.;
Adelson, P. David;
Shih-Shan Lang;
Grabb, Paul;
Greene, Stephanie;
Johnston, James M.;
Leonard, Jeffrey;
Magge, Suresh N.;
Marupudi, Neena I.;
Piatt, Joseph;
De Oliveira Sillero, Rafael;
Smith, Edward R.;
Smith, Jodi;
Strahle, Jennifer M.;
Vadivelu, Sudhakar;
Wellons III, John C.;
Wrubel, David;
Hatem, Asmaa;
Moody, Ciarra

Publication type:

Article

Shunt infection prevention practices in Hydrocephalus Clinical Research Network--Quality: a new quality improvement network for hydrocephalus management.

Published in:

Journal of Neurosurgery: Pediatrics, 2024, v. 33, n. 2, p. 157, doi. 10.3171/2023.10.PEDS23297

By:

Tamber, Mandeep S.;
Jensen, Hailey;
Clawson, Jason;
Nunn, Nichol;
Wellons III, John C.;
Smith, Jodi;
Martin, Jonathan E.;
Kestle, John R. W.

Publication type:

Article

Hydrocephalus surveillance following CSF diversion: a modified Delphi study.

Published in:

Journal of Neurosurgery: Pediatrics, 2022, v. 30, n. 2, p. 177, doi. 10.3171/2022.5.PEDS22116

By:

Hersh, David S.;
Martin, Jonathan E.;
Bristol, Ruth E.;
Browd, Samuel R.;
Grant, Gerald;
Gupta, Nalin;
Hankinson, Todd C.;
Jackson, Eric M.;
Kestle, John R. W.;
Krieger, Mark D.;
Kulkarni, Abhaya V.;
Madura, Casey J.;
Pindrik, Jonathan;
Pollack, Ian F.;
Raskin, Jeffrey S.;
Riva-Cambrin, Jay;
Rozzelle, Curtis J.;
Smith, Jodi L.;
Wellons III, John C.

Publication type:

Article

Standardization of shunt valves: one size does not fit all.

Published in:

Journal of Neurosurgery: Pediatrics, 2021, v. 28, n. 6, p. 745, doi. 10.3171/2021.4.PEDS21188

By:

Fulkerson, Daniel H.;
Smith, Jodi L.

Publication type:

Article

Increased Prevalence of Sensory Processing Issues in Pediatric Gastrointestinal Patient Population.

Published in:

Permanente Journal, 2022, v. 26, n. 4, p. 69, doi. 10.7812/TPP/22.071

By:

Wood, Jessica K.;
Garcia, Kara E.;
Carey, Rebecca G.

Publication type:

Article

Catch‐down growth in infants born large for gestational age.

Published in:

Nutrition in Clinical Practice, 2021, v. 36, n. 6, p. 1215, doi. 10.1002/ncp.10727

By:

Dunn, Rachel K.;
Uhing, Michael;
Goday, Praveen S.

Publication type:

Article

Two Case Studies and A Review of Paroxysmal Cold Hemoglobinuria.

Published in:

Laboratory Medicine, 2014, v. 45, n. 3, p. 253, doi. 10.1309/LMWD51B2KIFSBLBJ

By:

Davisson, Suzanne M.;
Slemp, Stephanie N.;
Slayten, Jayanna;
Cipkala, Douglas A.;
Waxman, Dan A.

Publication type:

Article

AAML0523: A report from the Children's Oncology Group on the efficacy of clofarabine in combination with cytarabine in pediatric patients with recurrent acute myeloid leukemia.

Published in:

Cancer (0008543X), 2014, v. 120, n. 16, p. 2482, doi. 10.1002/cncr.28674

By:

Cooper, Todd M.;
Alonzo, Todd A.;
Gerbing, Robert B.;
Perentesis, John P.;
Whitlock, James A.;
Taub, Jeffrey W.;
Horton, Terzah M.;
Gamis, Alan S.;
Meshinchi, Soheil;
Loken, Michael R.;
Razzouk, Bassem I.

Publication type:

Article

Favorable survival maintained in children who have myeloid leukemia associated with Down syndrome using reduced-dose chemotherapy on Children's Oncology Group trial A2971.

Published in:

Cancer (0008543X), 2012, v. 118, n. 19, p. 4806, doi. 10.1002/cncr.27484

By:

Sorrell, April D.;
Alonzo, Todd A.;
Hilden, Joanne M.;
Gerbing, Robert B.;
Loew, Thomas W.;
Hathaway, Lois;
Barnard, Dorothy;
Taub, Jeffrey W.;
Ravindranath, Yaddanapudi;
Smith, Franklin O.;
Arceci, Robert J.;
Woods, William G.;
Gamis, Alan S.

Publication type:

Article

Evaluation and Management of Hearing Loss in Survivors of Childhood and Adolescent Cancers: A Report From the Children's Oncology Group.

Published in:

2016

By:

Bass, Johnnie K.;
Knight, Kristin R.;
Yock, Torunn I.;
Chang, Kay W.;
Cipkala, Douglas;
Grewal, Satkiran S.

Publication type:

journal article

Treatment of two cases with refractory, metastatic intermediate-risk neuroblastoma with isotretenoin alone or observation.

Published in:

Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1104, doi. 10.1002/pbc.24889

By:

Pinto, Navin;
Cipkala, Douglas A.;
Ladd, Patricia E.;
Pu, Yonglin;
Cohn, Susan L.

Publication type:

Article

Phase I/II trial of clofarabine and cytarabine in children with relapsed/refractory acute lymphoblastic leukemia (AAML0523): A report from the Children's Oncology Group.

Published in:

Pediatric Blood & Cancer, 2013, v. 60, n. 7, p. 1141, doi. 10.1002/pbc.24398

By:

Cooper, Todd M.;
Razzouk, Bassem I.;
Gerbing, Robert;
Alonzo, Todd A.;
Adlard, Kathleen;
Raetz, Elizabeth;
Gamis, Alan S.;
Perentesis, John;
Whitlock, James A.

Publication type:

Article

MLL gene rearrangements in infant leukemia vary with age at diagnosis and selected demographic factors: A Children's Oncology Group (COG) study.

Published in:

Pediatric Blood & Cancer, 2012, v. 58, n. 6, p. 836, doi. 10.1002/pbc.23274

By:

Sam, Thien N.;
Kersey, John H.;
Linabery, Amy M.;
Johnson, Kimberly J.;
Heerema, Nyla A.;
Hilden, Joanne M.;
Davies, Stella M.;
Reaman, Gregory H.;
Ross, Julie A.

Publication type:

Article

Increasing diversity in pediatric hematology/oncology.

Published in:

Pediatric Blood & Cancer, 2011, v. 57, n. 1, p. 147, doi. 10.1002/pbc.22977

By:

Frugé, Ernest;
Lakoski, Joan M.;
Luban, Naomi;
Lipton, Jeffrey M.;
Poplack, David G.;
Hagey, Anne;
Felgenhauer, Judy;
Hilden, Joanne;
Margolin, Judith;
Vaiselbuh, Sarah R.;
Sakamoto, Kathleen M.

Publication type:

Article

Infant leukemia and congenital abnormalities: A Children's Oncology Group study.

Published in:

Pediatric Blood & Cancer, 2010, v. 55, n. 1, p. 95, doi. 10.1002/pbc.22495

By:

Johnson, Kimberly J.;
Roesler, Michelle A.;
Linabery, Amy M.;
Hilden, Joanne M.;
Davies, Stella M.;
Ross, Julie A.

Publication type:

Article

Medication Use in Schools.

Published in:

Journal of Pediatric Pharmacology & Therapeutics, 2020, v. 25, n. 2, p. 163, doi. 10.5863/1551-6776-25.2.163

By:

Phan, Hanna;
Butler, Susan M.;
Tobison, Jennifer;
Boucher, Elizabeth A.

Publication type:

Article

Impact of a Process Change on Prevalence of Prescribed Unmeasurable Liquid Doses in a Neonatal Intensive Care Unit.

Published in:

Journal of Pediatric Pharmacology & Therapeutics, 2020, v. 25, n. 2, p. 96, doi. 10.5863/1551-6776-25.2.96

By:

Zahn, Stephanie O.;
Tobison, Jennifer H.;
Place, Amanda J.;
Casey, Jamalyn N.;
Hess, Liz;
Foster, Todd

Publication type:

Article

Medication Use in Schools: Current Trends, Challenges, and Best Practices.

Published in:

Journal of Pediatric Pharmacology & Therapeutics, 2020, v. 25, n. 1, p. 7, doi. 10.5863/1551-6776-25.1.7

By:

Butler, Susan M.;
Boucher, Elizabeth A.;
Tobison, Jennifer;
Phan, Hanna

Publication type:

Article

Pediatric Pharmacists' Participation in Cardiopulmonary Resuscitation Events.

Published in:

Journal of Pediatric Pharmacology & Therapeutics, 2018, v. 23, n. 6, p. 502, doi. 10.5863/1551-6776-23.6.502

By:

Johnson, Peter N.;
Steele, Amy Mitchell-Van;
Nguyen, Amy L.;
Stoffell, Sylvia;
Whitmore, J. Maria

Publication type:

Article

A Multicenter Study Using the SWAG Scale to Compare Secondary Alveolar Bone Graft Outcomes for Patients With Cleft Lip and Palate.

Published in:

Cleft Palate Craniofacial Journal, 2016, v. 53, n. 2, p. 180, doi. 10.1597/14-215

By:

Russell, Kathleen;
Long, Ross E.;
Daskalogiannakis, John;
Mercado, Ana;
Hathaway, Ronald;
Semb, Gunvor;
Shaw, William

Publication type:

Article

The Americleft Study: An Inter--Center Study of Treatment Outcomes for Patients With Unilateral Cleft Lip and Palate Part 1. Principles and Study Design.

Published in:

Cleft Palate Craniofacial Journal, 2011, v. 48, n. 3, p. 239, doi. 10.1597/09-180.1

By:

Long, Ross E;
Hathaway, Ronald;
Daskalogiannakis, John;
Mercado, Ana;
Russell, Kathleen;
Cohen, Marilyn;
Semb, Gunvor;
Shaw, William

Publication type:

Article

The Americleft Study: An Inter--Center Study of Treatment Outcomes for Patients With Unilateral Cleft Lip and Palate Part 2. Dental Arch Relationships.

Published in:

Cleft Palate Craniofacial Journal, 2011, v. 48, n. 3, p. 244, doi. 10.1597/09-181.1

By:

Hathaway, Ronald;
Daskalogiannakis, John;
Mercado, Ana;
Russell, Kathleen;
Long, Ross E;
Cohen, Marilyn;
Semb, Gunvor;
Shaw, William

Publication type:

Article

The Americleft Study: An Inter--Center Study of Treatment Outcomes for Patients With Unilateral Cleft Lip and Palate Part 3. Analysis of Craniofacial Form.

Published in:

Cleft Palate Craniofacial Journal, 2011, v. 48, n. 3, p. 252, doi. 10.1597/09-185.1

By:

Daskalogiannakis, John;
Mercado, Ana;
Russell, Kathleen;
Hathaway, Ronald;
Dugas, Gregory;
Long, Ross E;
Cohen, Marilyn;
Semb, Gunvor;
Shaw, William

Publication type:

Article

The Americleft Study: An Inter--Center Study of Treatment Outcomes for Patients With Unilateral Cleft Lip and Palate Part 4. Nasolabial Aesthetics.

Published in:

Cleft Palate Craniofacial Journal, 2011, v. 48, n. 3, p. 259, doi. 10.1597/09-186.1

By:

Mercado, Ana;
Russell, Kathleen;
Hathaway, Ronald;
Daskalogiannakis, John;
Sadek, Hani;
Long, Ross E;
Cohen, Marilyn;
Semb, Gunvor;
Shaw, William

Publication type:

Article

The Americleft Study: An Inter--Center Study of Treatment Outcomes for Patients With Unilateral Cleft Lip and Palate Part 5. General Discussion and Conclusions.

Published in:

Cleft Palate Craniofacial Journal, 2011, v. 48, n. 3, p. 265, doi. 10.1597/09-187.1

By:

Russell, Kathleen;
Long, Ross E;
Hathaway, Ronald;
Daskalogiannakis, John;
Mercado, Ana;
Cohen, Marilyn;
Semb, Gunvor;
Shaw, William

Publication type:

Article

Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomesHuman Molecular Genetics, Vol. 00, No. 0Human Molecular Genetics, Vol. 00, No. 0.

Published in:

Human Molecular Genetics, 2018, v. 27, n. 21, p. 3710, doi. 10.1093/hmg/ddy287

By:

Whitley, Brittany N;
Lam, Christina;
Cui, Hong;
Haude, Katrina;
Bai, Renkui;
Escobar, Luis;
Hamilton, Afifa;
Brady, Lauren;
Tarnopolsky, Mark A;
Dengle, Lauren

Publication type:

Article

Case Report: Six-Year-Old Girl With Recurrent Episodes of Blue Toes.

Published in:

2010

By:

Kearby, Rachel;
Bowyer, Suzanne;
Sharrer, Julie;
Sharathkumar, Anjali

Publication type:

Case Study

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.

Published in:

Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00900-3

By:

Mannucci, Ilaria;
Dang, Nghi D. P.;
Huber, Hannes;
Murry, Jaclyn B.;
Abramson, Jeff;
Althoff, Thorsten;
Banka, Siddharth;
Baynam, Gareth;
Bearden, David;
Beleza-Meireles, Ana;
Benke, Paul J.;
Berland, Siren;
Bierhals, Tatjana;
Bilan, Frederic;
Bindoff, Laurence A.;
Braathen, Geir Julius;
Busk, Øyvind L.;
Chenbhanich, Jirat;
Denecke, Jonas;
Escobar, Luis F.

Publication type:

Article

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.

Published in:

Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00900-3

By:

Mannucci, Ilaria;
Dang, Nghi D. P.;
Huber, Hannes;
Murry, Jaclyn B.;
Abramson, Jeff;
Althoff, Thorsten;
Banka, Siddharth;
Baynam, Gareth;
Bearden, David;
Beleza-Meireles, Ana;
Benke, Paul J.;
Berland, Siren;
Bierhals, Tatjana;
Bilan, Frederic;
Bindoff, Laurence A.;
Braathen, Geir Julius;
Busk, Øyvind L.;
Chenbhanich, Jirat;
Denecke, Jonas;
Escobar, Luis F.

Publication type:

Article

Cleft lip/palate associated with 17p13.3 duplication involving a single candidate gene ( YWHAE).

Published in:

Clinical Genetics, 2014, v. 85, n. 6, p. 600, doi. 10.1111/cge.12237

By:

Tucker, M.E.;
Escobar, L.F.

Publication type:

Article

Growth hormone deficiency in megalencephaly‐capillary malformation syndrome: An association with activating mutations in PIK3CA.

Published in:

American Journal of Medical Genetics. Part A, 2020, v. 182, n. 1, p. 162, doi. 10.1002/ajmg.a.61403

By:

Davis, Shanlee;
Ware, Meredith A.;
Zeiger, Jordan;
Deardorff, Matthew A.;
Grand, Katheryn;
Grimberg, Adda;
Hsu, Stephanie;
Kelsey, Megan;
Majidi, Shideh;
Matthew, Revi P.;
Napier, Melanie;
Nokoff, Natalie;
Prasad, Chitra;
Riggs, Andrew C.;
McKinnon, Margaret L.;
Mirzaa, Ghayda

Publication type:

Article

Invited commentary: His life was lost but his heart still beats: In honor of children harmed by child abuse.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 12, p. 2329, doi. 10.1002/ajmg.a.61348

By:

Shur, Natasha;
Hinds, Tanya;
Shalaby‐Rana, Eglal;
Tinkle, Brad;
Frasier, Lori;
Bulas, Dorothy;
Summar, Marshall;
Jackson, Allison

Publication type:

Article

Response to letter, broken bones, and irresponsible testimony: Enough is enough already: The flawed Ehlers–Danlos syndrome infant fragility theory should not rule.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 12, p. 2335, doi. 10.1002/ajmg.a.61347

By:

Shur, Natasha;
Tinkle, Brad;
Summar, Marshall;
Frasier, Lori;
Shalaby‐Rana, Eglal;
McIntosh, Bruce

Publication type:

Article

Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 7, p. 1276, doi. 10.1002/ajmg.a.61173

By:

Stolerman, Elliot S.;
Francisco, Elizabeth;
Stallworth, Jennifer L.;
Jones, Julie R.;
Monaghan, Kristin G.;
Keller‐Ramey, Jennifer;
Person, Richard;
Wentzensen, Ingrid M.;
McWalter, Kirsty;
Keren, Boris;
Heron, Benedicte;
Nava, Caroline;
Heron, Delphine;
Kim, Katherine;
Burton, Barbara;
Al‐Musafri, Fatima;
O'Grady, Lauren;
Sahai, Inderneel;
Escobar, Luis F.;
Meuwissen, Marije

Publication type:

Article

SMARCE1, a rare cause of Coffin-Siris Syndrome: Clinical description of three additional cases.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 1967, doi. 10.1002/ajmg.a.37722

By:

Zarate, Yuri A.;
Bhoj, Elizabeth;
Kaylor, Julie;
Li, Dong;
Tsurusaki, Yoshinori;
Miyake, Noriko;
Matsumoto, Naomichi;
Phadke, Shubha;
Escobar, Luis;
Irani, Afifa;
Hakonarson, Hakon;
Schrier Vergano, Samantha A.

Publication type:

Article

Investigation of NRXN1 deletions: Clinical and molecular characterization.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 717, doi. 10.1002/ajmg.a.35780

By:

Dabell, Mindy Preston;
Rosenfeld, Jill A.;
Bader, Patricia;
Escobar, Luis F.;
El‐Khechen, Dima;
Vallee, Stephanie E.;
Dinulos, Mary Beth Palko;
Curry, Cynthia;
Fisher, Jamie;
Tervo, Raymond;
Hannibal, Mark C.;
Siefkas, Kiana;
Wyatt, Philip R.;
Hughes, Lauren;
Smith, Rosemarie;
Ellingwood, Sara;
Lacassie, Yves;
Stroud, Tracy;
Farrell, Sandra A.;
Sanchez‐Lara, Pedro A.

Publication type:

Article

Indiana Medical Resident's Knowledge of Surrogate Decision Making Laws.

Published in:

Community Health Equity Research & Policy, 2022, v. 42, n. 4, p. 361, doi. 10.1177/0272684X211004737

By:

Bartlett, Stephanie;
Fettig, Lyle P.;
Baenziger, Peter H.;
DiOrio, Eliana N.;
Herget, Kayla M.;
D'Cruz, Lynn;
Coughlin, Johanna R.;
Lake, Mikaela;
Truong, Amy;
Comer, Amber R.

Publication type:

Article

Ehlers–Danlos syndromes, hypermobility spectrum disorders, and associated co‐morbidities: Reports from EDS ECHO.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2021, v. 187, n. 4, p. 413, doi. 10.1002/ajmg.c.31954

By:

Hakim, Alan J.;
Tinkle, Brad T.;
Francomano, Clair A.

Publication type:

Article

Nurse manager succession planning: synthesis of the evidence.

Published in:

Journal of Nursing Management, 2013, v. 21, n. 7, p. 971, doi. 10.1111/jonm.12179

By:

Titzer, Jennifer;
Phillips, Tracy;
Tooley, Stephanie;
Hall, Norma;
Shirey, Maria

Publication type:

Article

Intrapulmonary recombinant FVIIa in neonatal ECMO‐associated alveolar hemorrhage.

Published in:

Pediatric Blood & Cancer, 2024, v. 71, n. 8, p. 1, doi. 10.1002/pbc.31130

By:

Han, Jennifer H.;
Kroeger, Ashley;
Beardsley, Andrew;
Garries, Emily;
Whitmore, Maria;
Kumar, Manjusha;
Sichting, Kay

Publication type:

Article

Prognostic significance of chromosomal abnormalities at relapse in children with relapsed acute myeloid leukemia: A retrospective cohort study of the Relapsed AML 2001/01 Study.

Published in:

Pediatric Blood & Cancer, 2022, v. 69, n. 1, p. 1, doi. 10.1002/pbc.29341

By:

Klein, Kim;
Beverloo, H. Berna;
Zimmermann, Martin;
Raimondi, Susana C.;
von Neuhoff, Christine;
de Haas, Valérie;
van Weelderen, Romy;
Cloos, Jacqueline;
Abrahamsson, Jonas;
Bertrand, Yves;
Dworzak, Michael;
Fynn, Alcira;
Gibson, Brenda;
Ha, Shau‐Yin;
Harrison, Christine J.;
Hasle, Henrik;
Elitzur, Sarah;
Leverger, Guy;
Maschan, Alexei;
Razzouk, Bassem

Publication type:

Article

Osteogenesis Imperfecta.

Published in:

Clinician Reviews, 2007, v. 17, n. 12, p. 47

By:

Burman, Tara L.;
Kayes, Kosmas J.

Publication type:

Article

Anisotropic Polytetrafluoroethylene Cardiovascular Conduits Spontaneously Expand in a Growing Lamb Model.

Published in:

Journal of Investigative Surgery, 2021, v. 34, n. 12, p. 1348, doi. 10.1080/08941939.2020.1805056

By:

Azakie, Anthony;
Carney, John P.;
Lahti, Matthew T.;
Moklyak, Yuriy;
Bianco, Richard W.

Publication type:

Article