Search Results - "SEIF, Fritz J"

Carl Liebermeister (1833-1901): a pioneer of the investigation and treatment of fever and the developer of a statistical test by Seneta, Eugene, Seif, Fritz J, Liebermeister, Hermann, Dietz, Klaus

“…In the second half of the nineteenth century, when the typical course of various febrile clinical phenomena was found to be specific to particular infectious…”
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Homozygous mutation within the conserved Ala-Phe-Asn-Glu-Thr motif of exon 7 of the LH receptor causes male pseudohermaphroditism by Gromoll, J, Schulz, A, Borta, H, Gudermann, T, Teerds, KJ, Greschniok, A, Nieschlag, E, Seif, FJ

“…BACKGROUND: Human chorionic gonadotropin/luteinizing hormone (hCG/LH) function in the male is mediated by the LH receptor (LHR) and is crucial for the normal…”
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Manifestation of thyroid autoimmunity in patients successfully treated for hypercortisolism by Müssig, Karsten, Gallwitz, Baptist, Häring, Hans-Ulrich, Seif, Fritz J.

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17α-Hydroxylase/17,20-Lyase Deficiency Caused by a Novel Homozygous Mutation (Y27Stop) in the Cytochrome CYP17 Gene by Müssig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F., Wudy, Stefan A., Schnauder, Günter, Häring, Hans-Ulrich, Seif, Fritz J., Gallwitz, Baptist

“…Context: 17α-Hydroxylase/17,20-lyase deficiency, a rare autosomal recessive form of congenital adrenal hyperplasia, is caused by mutations in the cytochrome…”
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17 alpha -Hydroxylase/17,20-Lyase Deficiency Caused by a Novel Homozygous Mutation (Y27Stop) in the Cytochrome CYP17 Gene by Muessig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F, Wudy, Stefan A, Schnauder, Guenter, Haering, Hans-Ulrich, Seif, Fritz J, Gallwitz, Baptist

“…CONTEXT: 17 alpha -Hydroxylase/17,20-lyase deficiency, a rare autosomal recessive form of congenital adrenal hyperplasia, is caused by mutations in the…”
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17alpha-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27Stop) in the cytochrome CYP17 gene by Müssig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F, Wudy, Stefan A, Schnauder, Günter, Häring, Hans-Ulrich, Seif, Fritz J, Gallwitz, Baptist

“…17alpha-Hydroxylase/17,20-lyase deficiency, a rare autosomal recessive form of congenital adrenal hyperplasia, is caused by mutations in the cytochrome P450c17…”
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17a-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27stop) in the cytochrome CYP17 gene by MÜSSIG, Karsten, KALTENBACH, Simone, MACHICAO, Fausto, MASER-GLUTH, Christiane, HARTMANN, Michaela F, WUDY, Stefan A, SCHNAUDER, Günter, HÄRING, Hans-Ulrich, SEIF, Fritz J, GALLWITZ, Baptist

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The natural course of multiple endocrine neoplasia type IIb. A study of 18 cases by Vasen, H F, van der Feltz, M, Raue, F, Kruseman, A N, Koppeschaar, H P, Pieters, G, Seif, F J, Blum, W F, Lips, C J

“…Multiple endocrine neoplasia (MEN) type IIb is an autosomal dominantly inherited disorder associated with medullary thyroid cancer, pheochromocytoma, and a…”
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Analysis of thyroid stimulating hormone-receptor mutations by temperature-gradient gel electrophoresis by Koch, M, Wahl, R, Seif, F J

“…Somatic mutations in the genes for G-protein-coupled receptors which regulate intracellular levels of cyclic AMP have been found in several regions coding for…”
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Manifestation of thyroid autoimmunity in patients successfully treated for hypercortisolism by Müssig, Karsten, Gallwitz, Baptist, Häring, Hans-Ulrich, Seif, Fritz J

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Demaskierung einer sekundären Nebennieren-rindeninsuffizienz und eines Diabetes insipidus centralis durch eine hochfieberhafte akute Hantaan-Virus-Infektion by Schröder, Stephen, Dilger, Jörg, Weiss, Eva-Maria, Seif, Fritz J.

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