Comparing Adaptive Radiations Across Space, Time, and Taxa von Gillespie, RG, Bennett, GM, De Meester, L, Feder, JL, Fleischer, RC, Harmon, LJ, Hendry, AP, Knope, ML, Mallet, J, Martin, C, Parent, CE, Patton, AH, Pfennig, KS, Rubinoff, D, Schluter, D, Seehausen, O, Shaw, KL, Stacy, E, Stervander, M, Stroud, JT, Wagner, C, Wogan, GOU

Volltext bestellen

Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development von Simpson, M.A., Hsu, R., Keir, L.S., Hao, J., Sivapalan, G., Ernst, L.M., Zackai, E.H., Al-Gazali, L.I., Hulskamp, G., Kingston, H.M., Prescott, T.E., Ion, A., Patton, M.A., Murday, V., George, A., Crosby, A.H.

Volltext

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome von Tartaglia, Marco, Mehler, Ernest L., Goldberg, Rosalie, Zampino, Giuseppe, Brunner, Han G., Kremer, Hannie, van der Burgt, Ineke, Crosby, Andrew H., Ion, Andra, Jeffery, Steve, Kalidas, Kamini, Patton, Michael A., Kucherlapati, Raju S., Gelb, Bruce D.

Volltext

Estimates of the global, regional, and national morbidity, mortality, and aetiologies of lower respiratory tract infections in 195 countries: a systematic analysis for the Global B... von Troeger, Christopher, Forouzanfar, Mohammad, Rao, Puja C, Khalil, Ibrahim, Brown, Alexandria, Swartz, Scott, Fullman, Nancy, Mosser, Jonathan, Thompson, Robert L, Reiner, Robert C, Abajobir, Amanuel, Alam, Noore, Alemayohu, Mulubirhan Assefa, Amare, Azmeraw T, Antonio, Carl Abelardo, Asayesh, Hamid, Avokpaho, Euripide, Barac, Aleksandra, Beshir, Muktar A, Boneya, Dube Jara, Brauer, Michael, Dandona, Lalit, Dandona, Rakhi, Fitchett, Joseph R A, Gebrehiwot, Tsegaye Tewelde, Hailu, Gessessew Buggsa, Hotez, Peter J, Kasaeian, Amir, Khoja, Tawfik, Kissoon, Niranjan, Knibbs, Luke, Kumar, G Anil, Rai, Rajesh Kumar, El Razek, Hassan Magdy Abd, Mohammed, Muktar S K, Nielson, Katie, Oren, Eyal, Osman, Abdalla, Patton, George, Qorbani, Mostafa, Roba, Hirbo Shore, Sartorius, Benn, Savic, Miloje, Shigematsu, Mika, Sykes, Bryan, Swaminathan, Soumya, Topor-Madry, Roman, Ukwaja, Kingsley, Werdecker, Andrea, Yonemoto, Naohiro, El Sayed Zaki, Maysaa, Lim, Stephen S, Naghavi, Mohsen, Vos, Theo, Hay, Simon I, Murray, Christopher J L, Mokdad, Ali H

Volltext

Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia von Simpson, MA, Scheuerle, A, Hurst, J, Patton, MA, Stewart, H, Crosby, AH

Volltext

Implant design influences patient outcome after total knee arthroplasty von Hamilton, D F, Burnett, R, Patton, J T, Howie, C R, Moran, M, Simpson, AH, Gaston, P

Volltext

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase von Simpson, Michael A, Cross, Harold, Proukakis, Christos, Priestman, David A, Neville, David C A, Reinkensmeier, Gabriele, Wang, Heng, Wiznitzer, Max, Gurtz, Kay, Verganelaki, Argyro, Pryde, Anna, Patton, Michael A, Dwek, Raymond A, Butters, Terry D, Platt, Frances M, Crosby, Andrew H

Volltext

Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia von Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.

Volltext

Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair von Simpson, M.A., Mansour, S., Ahnood, D., Kalidas, K., Patton, M.A., McKenna, W.J., Behr, E.R., Crosby, A.H.

Volltext

Lengthening the moment arm of the patella confers enhanced extensor mechanism power following total knee arthroplasty von Hamilton, David F., Simpson, A. Hamish R.W., Burnett, Richard, Patton, James T., Moran, Matthew, Clement, Nicholas D., Howie, Colin R., Gaston, Paul

Volltext

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia von Patel, Heema, Cross, Harold, Proukakis, Christos, Hershberger, Ruth, Bork, Peer, Ciccarelli, Francesca D., Patton, Michael A., McKusick, Victor A., Crosby, Andrew H.

Volltext

A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23 von DICK, K. J, AL-MJENI, Hons R, BASKIR, W, KOUL, R, SIMPSON, M. A, PATTON, M. A, RAEBURN, S, CROSBY, A. H

Volltext

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia von Ciccarelli, Francesca D, Proukakis, Christos, Patel, Heema, Cross, Harold, Azam, Shakil, Patton, Michael A, Bork, Peer, Crosby, Andrew H

Volltext

The Silver Syndrome Variant of Hereditary Spastic Paraplegia Maps to Chromosome 11q12-q14, with Evidence for Genetic Heterogeneity within This Subtype von Patel, H., Hart, P.E., Warner, T.T., Houlston, R.S., Patton, M.A., Jeffery, S., Crosby, A.H.

Volltext

Global, regional, and national burden of 12 mental disorders in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019 von Ferrari, AJ, Santomauro, DF, Herrera, AMM, Shadid, J, Ashbaugh, C, Erskine, HE, Charlson, FJ, Degenhardt, L, Scott, JG, McGrath, JJ, Allebeck, P, Benjet, C, Breitborde, NJK, Brugha, T, Dai, X, Dandona, L, Dandona, R, Fischer, F, Haagsma, JA, Maria Haro, J, Kieling, C, Knudsen, AKS, Kumar, GA, Leung, J, Majeed, A, Mitchell, PB, Moitra, M, Mokdad, AH, Molokhia, M, Patten, SB, Patton, GC, Phillips, MR, Soriano, JB, Stein, DJ, Stein, MB, Szoeke, CE, Naghavi, M, Hay, S, Murray, CJL, Vos, T, Whiteford, HA

Volltext

Ultrasensitive Human Immunodeficiency Virus Type 1 p24 Antigen Assay Modified for Use on Dried Whole-Blood Spots as a Reliable, Affordable Test for Infant Diagnosis von Patton, Janet C, Sherman, Gayle G, Coovadia, Ashraf H, Stevens, Wendy S, Meyers, Tammy M

Volltext

Troyer syndrome revisited: A clinical and radiological study of a complicated hereditary spastic paraplegia von PROUKAKIS, Christos, CROSS, Harold, PATEL, Heema, PATTON, Michael A, VALENTINE, Alan, CROSBY, Andrew H

Volltext

P23 The health of malaysia’s adolescents: findings from the global burden of disease 2017 study von Abdul-Razak, S, Sawyer, S M, Patton, G C, Cini, K, NA, Ahmad, Mokdad, AH, Azzopardi, P S

Volltext

The health benefits of secondary education in adolescents and young adults: An international analysis in 186 low-, middle- and high-income countries from 1990 to 2013 von Viner, RM, Hargreaves, DS, Ward, J, Bonell, C, Mokdad, AH, Patton, G

Volltext

A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia von REED, Johanna A, WILKINSON, Phillip A, PATEL, Heema, SIMPSON, Michael A, CHATONNET, Arnaud, ROBAY, Dimitri, PATTON, Michael A, CROSBY, Andrew H, WARNER, Thomas T

Volltext