Gerd Schmitz

Neonatal Respiratory Insufficiency Caused by an (Homozygous) ABCA3-Stop Mutation: a Systematic Evaluation of Therapeutic Options

G. Schmitz, K. Poplawska, M. Griese, 2014, Klinische Pädiatrie.

Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonate

J. Poeschl, G. Schmitz, M. Griese, 2011, BMJ Case Reports.

Skoura – a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene

N. Kfir, M. Khayat, T. Falik-Zaccai, 2009, Clinical genetics.