Search Results - Schnieders, Birgit

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  1. 1
    Seltene Erkrankungen und Digitalisierung im Kontext des Nationalen Aktionsbündnisses für Menschen mit Seltenen Erkrankungen (NAMSE)

    Seltene Erkrankungen und Digitalisierung im Kontext des Nationalen Aktionsbündnisses für Menschen mit Seltenen Erkrankungen (NAMSE) by Wessel, Theda, Heuing, Katharina, Schlangen, Miriam, Schnieders, Birgit, Algermissen, Markus

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  2. 2
    Seltene Erkrankungen und Digitalisierung im Kontext des Nationalen Aktionsbündnisses für Menschen mit Seltenen Erkrankungen (NAMSE)

    Seltene Erkrankungen und Digitalisierung im Kontext des Nationalen Aktionsbündnisses für Menschen mit Seltenen Erkrankungen (NAMSE) by Wessel, Theda, Heuing, Katharina, Schlangen, Miriam, Schnieders, Birgit, Algermissen, Markus

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  3. 3
    Seven years of the National Action League for People with Rare Diseases : NAMSE - a success story?!

    Seven years of the National Action League for People with Rare Diseases : NAMSE - a success story?! by Halbach, Alexandra, Schnieders, Birgit, Knufmann-Happe, Karin

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  4. 4
    Rare diseases, digitization, and the National Action League for People with Rare Diseases (NAMSE)

    Rare diseases, digitization, and the National Action League for People with Rare Diseases (NAMSE) by Wessel, Theda, Heuing, Katharina, Schlangen, Miriam, Schnieders, Birgit, Algermissen, Markus

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  5. 5
    7 Jahre Nationales Aktionsbündnis für Menschen mit Seltenen Erkrankungen: NAMSE – ein Erfolgsmodell?

    7 Jahre Nationales Aktionsbündnis für Menschen mit Seltenen Erkrankungen: NAMSE – ein Erfolgsmodell? by Halbach, Alexandra, Schnieders, Birgit, Knufmann-Happe, Karin

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  6. 6
    7 Jahre Nationales Aktionsbündnis für Menschen mit Seltenen Erkrankungen

    7 Jahre Nationales Aktionsbündnis für Menschen mit Seltenen Erkrankungen by Halbach, Alexandra, Schnieders, Birgit, Knufmann-Happe, Karin

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  7. 7
    Developing a national plan for rare diseases in Germany through concerted action: the national action league for people with rare diseases

    Developing a national plan for rare diseases in Germany through concerted action: the national action league for people with rare diseases by Héon-Klin, Véronique, Halbach, Alexandra, Schlangen, Miriam, Schnieders, Birgit

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  8. 8
    Report of an International Survey of Molecular Genetic Testing Laboratories

    Report of an International Survey of Molecular Genetic Testing Laboratories by McGovern, Margaret M., Elles, Rob, Beretta, Isabella, Somerville, Martin J., Hoefler, Gerald, Keinanen, Mauri, Barton, David, Carson, Nancy, Dequeker, Elisabeth, Brdicka, Radim, Blazkova, Alena, Aymé, Ségolène, Schnieders, Birgit, Müller, Clemens R., Dalen, Vibeke, Martinez, Armando Albert, Kristoffersson, Ulf, Ozguc, Meral, Mueller, Hansjakob, Boone, Joe, Lubin, Ira M., Sequeiros, Jorge, Taruscio, Domenica, Williamson, Bob, Mainland, Lynn, Yoshikura, Hiroshi, Ronchi, Elettra

    Published in Community genetics
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  9. 9
    Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the β-subunit of the mitochondrial trifunctional protein gene leads to failure of long-chain fatty acid β-oxidation with fatal outcome

    Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the β-subunit of the mitochondrial trifunctional protein gene leads to failure of long-cha... by SCHWAB, Karl Otfried, ENSENAUER, Regina, MATERN, Dietrich, UYANIK, Gökhan, SCHNIEDERS, Birgit, WANDERS, Ronald J. A, LEHNERT, Willy

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  10. 10
    Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the [beta]-subunit of the mitochondrial trifunctional protein gene leads to failure of long-chain fatty acid [beta]-oxidation with fatal outcome

    Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the [beta]-subunit of the mitochondrial trifunctional protein gene leads to failure of lon... by Schwab, Karl, Ensenauer, Regina, Matern, Dietrich, Uyanik, Gökhan, Schnieders, Birgit, Wanders, Ronald J, Lehnert, Willy

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  11. 11
    Mapping of a gene for familial juvenile nephronophthisis : refining the map and defining flanking markers on chromosome 2

    Mapping of a gene for familial juvenile nephronophthisis : refining the map and defining flanking markers on chromosome 2 by HILDEBRANDT, F, SINGH-SAWHNEY, I, WEBER, J. L, BRANDIS, M, SCHNIEDERS, B, CENTOFANTE, L, OMRAN, H, POHLMANN, A, SCHMALTZ, C, WEDEKIND, H, SCHUBOTZ, C, ANTIGNAC, C

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  12. 12
    Bioorganometallic Chemistry: Reactions of Methyltitanocene Cation Complexes with a Singly Deprotected Methyl Glucopyranoside

    Bioorganometallic Chemistry: Reactions of Methyltitanocene Cation Complexes with a Singly Deprotected Methyl Glucopyranoside by Meyer zu Berstenhorst, Birgit, Erker, Gerhard, Kehr, Gerald, Wasilke, Julia-Christina, Müller, Jens, Redlich, Hartmut, Pyplo-Schnieders, Jutta

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