Survival in Duchenne muscular dystrophy

Por RALL, SUSANNE, GRIMM, TIEMO
Publicado em 2012

Risk assessment and genetic counseling in families with Duchenne muscular dystrophy

Por GRIMM, TIEMO, KRESS, WOLFRAM, MENG, GERHARD, MÜLLER, CLEMENS R.
Publicado em 2012

Reply to Goodship et al

Por Koch, Manuela C., Grimm, Tiemo, Harley, Helen G., Harper, Peter S.
Publicado em 1992

Reply to Poulton

Por Koch, Manuela C., Grimm, Tiemo, Harley, Helen G., Harper, Peter S.
Publicado em 1992

Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a SOD-1 Mutation: Potential Impact of CNTF as a Candidate Modifier Gene

Por Giess, Ralf, Holtmann, Bettina, Braga, Massimiliano, Grimm, Tiemo, Müller-Myhsok, Bertram, Toyka, Klaus V., Sendtner, Michael
Publicado em 2002

PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption

Por Decker, Eva, Stellzig-Eisenhauer, Angelika, Fiebig, Britta S., Rau, Christiane, Kress, Wolfram, Saar, Kathrin, Rüschendorf, Franz, Hubner, Norbert, Grimm, Tiemo, Weber, Bernhard H.F.
Publicado em 2008

Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia

Por Bergmann, Carsten, Fliegauf, Manfred, Brüchle, Nadina Ortiz, Frank, Valeska, Olbrich, Heike, Kirschner, Jan, Schermer, Bernhard, Schmedding, Ingolf, Kispert, Andreas, Kränzlin, Bettina, Nürnberg, Gudrun, Becker, Christian, Grimm, Tiemo, Girschick, Gundula, Lynch, Sally A., Kelehan, Peter, Senderek, Jan, Neuhaus, Thomas J., Stallmach, Thomas, Zentgraf, Hanswalter, Nürnberg, Peter, Gretz, Norbert, Lo, Cecilia, Lienkamp, Soeren, Schäfer, Tobias, Walz, Gerd, Benzing, Thomas, Zerres, Klaus, Omran, Heymut
Publicado em 2008