Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency von Simm, Franziska, Griesbeck, Anne, Choukair, Daniela, Weiß, Birgit, Paramasivam, Nagarajan, Klammt, Jürgen, Schlesner, Matthias, Wiemann, Stefan, Martinez, Cristina, Hoffmann, Georg F., Pfäffle, Roland W., Bettendorf, Markus, Rappold, Gudrun A.

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PROP1 Mutations Cause Progressive Deterioration of Anterior Pituitary Function including Adrenal Insufficiency: A Longitudinal Analysis von Böttner, Antje, Keller, Eberhard, Kratzsch, Jürgen, Stobbe, Heike, Weigel, Johannes F. W., Keller, Alexandra, Hirsch, Wolfgang, Kiess, Wieland, Blum, Werner F., Pfäffle, Roland W.

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Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development von Mullen, Rachel D., Colvin, Stephanie C., Hunter, Chad S., Savage, Jesse J., Walvoord, Emily C., Bhangoo, Amrit P.S., Ten, Svetlana, Weigel, Johannes, Pfäffle, Roland W., Rhodes, Simon J.

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Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes von Blum, Werner F., Klammt, Jürgen, Amselem, Serge, Pfäffle, Heike M., Legendre, Marie, Sobrier, Marie-Laure, Luton, Marie-Pierre, Child, Christopher J., Jones, Christine, Zimmermann, Alan G., Quigley, Charmian A., Cutler, Gordon B., Deal, Cheri L., Lebl, Jan, Rosenfeld, Ron G., Parks, John S., Pfäffle, Roland W.

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A novel FoxD3 Variant Is Associated With Vitiligo and Elevated Thyroid Auto-Antibodies von Schunter, Jo Ana, Löffler, Dennis, Wiesner, Tobias, Kovacs, Peter, Badenhoop, Klaus, Aust, Gabriela, Tönjes, Anke, Müller, Peter, Baber, Ronny, Simon, Jan C, Führer, Dagmar, Pfäffle, Roland W, Thiery, Joachim, Stumvoll, Michael, Kiess, Wieland, Kratzsch, Jürgen, Körner, Antje

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Associations between Pituitary Imaging Abnormalities and Clinical and Biochemical Phenotypes in Children with Congenital Growth Hormone Deficiency: Data from an International Obser... von Deal, Cheri, Hasselmann, Caroline, Pfäffle, Roland W., Zimmermann, Alan G., Quigley, Charmian A., Child, Christopher J., Shavrikova, Elena P., Cutler Jr, Gordon B., Blum, Werner F.

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Mutations in PROP1 cause familial combined pituitary hormone deficiency von WEI WU, COGAN, J. D, PHILLIPS, J. A, ROSENFELD, M. G, PFÄFFLE, R. W, DASEN, J. S, FRISCH, H, O'CONNELL, S. M, FLYNN, S. E, BROWN, M. R, MULLIS, P. E, PARKS, J. S

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Longitudinal Imaging Reveals Pituitary Enlargement Preceding Hypoplasia in Two Brothers with Combined Pituitary Hormone Deficiency Attributable to PROP1 Mutation von Riepe, Felix G., Partsch, Carl-Joachim, Blankenstein, Oliver, Mönig, Heiner, Pfäffle, Roland W., Sippell, Wolfgang G.

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New N-terminal located mutation (Q4ter) within the POU1F1-gene ( PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype von Salemi, Souzan, Besson, Amélie, Eblé, Andrée, Gallati, Sabina, Pfäffle, Roland W, Mullis, Primus E

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Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomesResearch... von Werner F. Blum, Jürgen Klammt, Serge Amselem, Heike M. Pfäffle, Marie Legendre, Marie-Laure Sobrier, Marie-Pierre Luton, Christopher J. Child, Christine Jones, Alan G. Zimmermann, Charmian A. Quigley, Gordon B. Cutler, Jr, Cheri L. Deal, Jan Lebl, Ron G. Rosenfeld, John S. Parks, Roland W. Pfäffle

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Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation von RIEPE, Felix G, PARTSCH, Carl-Joachim, BLANKENSTEIN, Oliver, MÖNIG, Heiner, PFÄFFLE, Roland W, SIPPELL, Wolfgang G

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Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin β-subunit gene follows an autosomal recessive inheritance von DOEKER, B. M, PFÄFFLE, R. W, POHLENZ, J, ANDLER, W

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Congenital Central Hypothyroidism due to a Homozygous Mutation in the Thyrotropin β-Subunit Gene Follows an Autosomal Recessive Inheritance 1 von Doeker, Beate M., Pfäffle, Roland W., Pohlenz, Joachim, Andler, Werner

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Congenital Central Hypothyroidism due to a Homozygous Mutation in the Thyrotropin β-Subunit Gene Follows an Autosomal Recessive Inheritance1 von Doeker, Beate M, Pfäffle, Roland W, Pohlenz, Joachim, Andler, Werner

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Systems Biology von Pfäffle, Roland W.

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New Methods von Pfäffle, Roland W.

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Mutations in PROP 1 cause familial combined pituitary hormone deficiency von Wu, Wei, Cogan, Joy D, Pfäffle, Roland W, Dasen, Jeremy S, Frisch, Herwig, O'Connell1, Shawn M, Flynn, Sarah E, Brown, Milton R, Mullis, Primus E, Parks, John S, Phillips III, John A, Rosenfeld, Michael G

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Pit-1 and hypopituitarism von Parks, John S., Kinoshita, Ei-Ichi, Pfaffle, Roland W.

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Acceleration of skeletal maturation in Central Europe over the last two decades: insights from two cohorts of healthy children von Pape, Johanna, Rosolowski, Maciej, Zimmermann, Peter, Pfäffle, Roland, Hirsch, Franz W., Gräfe, Daniel

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IGF-I Receptor Mutations Resulting in Intrauterine and Postnatal Growth Retardation von Abuzzahab, M. Jennifer, Schneider, Anke, Goddard, Audrey, Grigorescu, Florin, Lautier, Corinne, Keller, Eberhard, Kiess, Wieland, Klammt, Jürgen, Kratzsch, Jürgen, Osgood, Doreen, Pfäffle, Roland, Raile, Klemens, Seidel, Berthold, Smith, Robert J, Chernausek, Steven D

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