|
🐜
|
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
16 auth.
K. Schlingmann,
S. Weber,
M. Peters,
L. N. Nejsum,
H. Vitzthum,
K. Klingel,
M. Kratz,
E. Haddad,
E. Ristoff,
D. Dinour,
...
M. Syrrou,
S. Nielsen,
M. Sassen,
S. Waldegger,
H. Seyberth,
M. Konrad
|
9 |
2002 |
9
🐜
|
|
🐬
|
Pharmacokinetics of different routes of administration of misoprostol.
O. Tang,
H. Schweer,
H. Seyberth,
Sharon W H Lee,
P. Ho
|
9 |
2002 |
9
🐬
|
|
🦁
|
Prostaglandins as mediators of hypercalcemia associated with certain types of cancer.
H. Seyberth,
G. Segre,
J. L. Morgan,
B. Sweetman,
J. Potts,
J. Oates
|
8 |
1975 |
8
🦁
|
|
🐜
|
Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia.
8 auth.
V. Chubanov,
S. Waldegger,
M. Mederos y Schnitzler,
H. Vitzthum,
M. Sassen,
H. Seyberth,
...
M. Konrad,
T. Gudermann
|
8 |
2004 |
8
🐜
|
|
🐜
|
Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis.
8 auth.
J. Gill,
Jurgen C. Fro¨lich,
R. Bowden,
A. Taylor,
H. Keiser,
H. Seyberth,
...
J. Oates,
F. Bartter
|
8 |
1976 |
8
🐜
|
|
🐜
|
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.
15 auth.
M. Konrad,
M. Vollmer,
H. Lemmink,
L. Heuvel,
N. Jeck,
R. Vargas-Poussou,
Alicia L. Lakings,
R. Ruf,
G. Deschênes,
C. Antignac,
...
L. Guay-Woodford,
N. Knoers,
H. Seyberth,
D. Feldmann,
F. Hildebrandt
|
8 |
2000 |
8
🐜
|
|
🐜
|
Salt wasting and deafness resulting from mutations in two chloride channels.
8 auth.
K. Schlingmann,
M. Konrad,
N. Jeck,
Petra Waldegger,
S. Reinalter,
M. Holder,
...
H. Seyberth,
S. Waldegger
|
7 |
2004 |
7
🐜
|
|
🐢
|
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.
8 auth.
M. Peters,
N. Jeck,
S. Reinalter,
A. Leonhardt,
B. Tönshoff,
Gunther Klaus,
...
M. Konrad,
H. Seyberth
|
7 |
2002 |
7
🐢
|
|
🐢
|
Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype
N. Jeck,
M. Konrad,
M. Peters,
S. Weber,
K. Bonzel,
H. Seyberth
|
7 |
2000 |
7
🐢
|
|
🦁
|
Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome.
H. Seyberth,
W. Rascher,
H. Schweer,
P. Kühl,
O. Mehls,
K. Schärer
|
7 |
1985 |
7
🦁
|
|
🦁
|
Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects
H. Seyberth,
K. Schlingmann
|
7 |
2011 |
7
🦁
|
