Works matching IS 17501172 AND DT 2008 AND VI 3


Results: 56
    1
    2
    3

    Monosomy 18p.

    Published in:
    2008
    By:
    • Turleau C;
    • Turleau, Catherine
    Publication type:
    journal article
    4

    Cluster headache.

    Published in:
    2008
    By:
    • Leroux E;
    • Ducros A;
    • Leroux, Elizabeth;
    • Ducros, Anne
    Publication type:
    journal article
    5
    6
    7
    8
    9
    10
    11
    12

    Leopard syndrome.

    Published in:
    2008
    By:
    • Sarkozy A;
    • Digilio MC;
    • Dallapiccola B;
    • Sarkozy, Anna;
    • Digilio, Maria Cristina;
    • Dallapiccola, Bruno
    Publication type:
    journal article
    13

    Gitelman syndrome.

    Published in:
    2008
    By:
    • Knoers NV;
    • Levtchenko EN;
    • Knoers, Nine V A M;
    • Levtchenko, Elena N
    Publication type:
    journal article
    14

    Alpha-mannosidosis.

    Published in:
    2008
    By:
    • Malm D;
    • Nilssen ø;
    • Malm, Dag;
    • Nilssen, Øivind
    Publication type:
    journal article
    15
    16

    Congenital long QT syndrome.

    Published in:
    2008
    By:
    • Crotti L;
    • Celano G;
    • Dagradi F;
    • Schwartz PJ;
    • Crotti, Lia;
    • Celano, Giuseppe;
    • Dagradi, Federica;
    • Schwartz, Peter J
    Publication type:
    journal article
    17
    18
    19
    20
    21
    22

    Syndromic (phenotypic) diarrhea in early infancy.

    Published in:
    2008
    By:
    • Goulet O;
    • Vinson C;
    • Roquelaure B;
    • Brousse N;
    • Bodemer C;
    • Cézard JP;
    • Goulet, Olivier;
    • Vinson, Christine;
    • Roquelaure, Bertrand;
    • Brousse, Nicole;
    • Bodemer, Christine;
    • Cézard, Jean-Pierre
    Publication type:
    journal article
    23
    24
    25
    26
    27

    Primary biliary cirrhosis.

    Published in:
    2008
    By:
    • Kumagi T;
    • Heathcote EJ;
    • Kumagi, Teru;
    • Heathcote, E Jenny
    Publication type:
    journal article
    28
    29

    Syndromic (phenotypic) diarrhea in early infancy.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-6
    By:
    • Goulet, Olivier;
    • Vinson, Christine;
    • Roquelaure, Bertrand;
    • Brousse, Nicole;
    • Bodemer, Christine;
    • Cézard, Jean-Pierre
    Publication type:
    Article
    30
    31
    32

    Brown-Vialetto-Van Laere syndrome.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-9
    By:
    • Sathasivam, Sivakumar
    Publication type:
    Article
    33

    Idiopathic pulmonary fibrosis.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-8
    By:
    • Meltzer, Eric B.;
    • Noble, Paul W.
    Publication type:
    Article
    34
    35
    36

    Malignant mesothelioma.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 34, doi. 10.1186/1750-1172-3-34
    Publication type:
    Article
    37
    38

    Multiple osteochondromas.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-3
    By:
    • Bovée, Judith V. M. G.
    Publication type:
    Article
    39

    Mixed cryoglobulinemia.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-25
    By:
    • Ferri, Clodoveo
    Publication type:
    Article
    40
    41

    Gitelman syndrome.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-22
    By:
    • Knoers, Nine V. A. M.;
    • Levtchenko, Elena N.
    Publication type:
    Article
    42

    Monosomy 18p.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-4
    By:
    • Turleau, Catherine
    Publication type:
    Article
    43

    Alpha-mannosidosis.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-21
    By:
    • Malm, Dag;
    • Nilssen, Øivind
    Publication type:
    Article
    44
    45

    Cluster headache.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-20
    By:
    • Leroux, Elizabeth;
    • Ducros, Anne
    Publication type:
    Article
    46
    47

    Congenital long QT syndrome.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-18
    By:
    • Crotti, Lia;
    • Celano, Giuseppe;
    • Dagradi, Federica;
    • Schwartz, Peter J.
    Publication type:
    Article
    48

    Acromegaly.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-17
    By:
    • Chanson, Philippe;
    • Salenave, Sylvie
    Publication type:
    Article
    49
    50

    Brachydactyly.

    Published in:
    Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-15
    By:
    • Temtamy, Samia A.;
    • Aglan, Mona S.
    Publication type:
    Article