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Results of search for 'au:"Rutishauser, J"'
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Authors
Beuret, N
Bider, M D
Burri, E
Böni, J
Böni-Schnetzler, M
Cathomas, G
Egger, S S
Froesch, E R
Funke, G
Futo, E
Gaskill, M B
Groeschl, I
Hailemariam, S
Hauri, C
Huisman, T
Hussain, M
Kopp, P
Rutishauser, J
Schmid, C
Zapf, J
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Topics
Adult
Aged
Animals
Arginine Vasopressin
Blood Glucose
Carrier Proteins
Diabetes Insipidus
Female
Humans
Insulin-Like Growth Factor Binding Proteins
Insulin-Like Growth Factor I
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Middle Aged
Mutation
Protein Precursors
Rats
blood
genetics
metabolism
pharmacology
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English
German
Your search returned 14 results.
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1.
[Treatment with statins: lowering of cholesterol or more?].
[electronic resource]
by
Rutishauser, J
Producer:
20060320
In:
Praxis
vol. 95
Online resources:
Available from publisher's website
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2.
Aquaporin-2 water channel mutations and nephrogenic diabetes insipidus: new variations on a theme.
[electronic resource]
by
Rutishauser, J
Kopp, P
Producer:
19990329
In:
European journal of endocrinology
vol. 140
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3.
Surprising news: a putative sulfate transporter is defective in Pendred's syndrome.
[electronic resource]
by
Rutishauser, J
Kopp, P
Producer:
19980805
In:
European journal of endocrinology
vol. 138
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4.
Hormone-inactive pituitary macroadenoma: an uncommon cause for the syndrome of inappropriate antidiuresis.
[electronic resource]
by
Groeschl, I
Kos, S
Rutishauser, J
Producer:
20080811
In:
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
vol. 116
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5.
The normoglycaemic patient with nephrotic syndrome.
[electronic resource]
by
Rutishauser, J
Hailemariam, S
Weinreich, T
Producer:
19980909
In:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
vol. 13
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6.
Streptococcal toxic shock syndrome in two patients infected by a colonized surgeon.
[electronic resource]
by
Rutishauser, J
Funke, G
Lütticken, R
Ruef, C
Producer:
20000727
In:
Infection
vol. 27
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7.
Mechanism of endoplasmic reticulum retention of mutant vasopressin precursor caused by a signal peptide truncation associated with diabetes insipidus.
[electronic resource]
by
Beuret, N
Rutishauser, J
Bider, M D
Spiess, M
Producer:
19990727
In:
The Journal of biological chemistry
vol. 274
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8.
Simultaneous bilateral spontaneous pneumothorax in a patient with recurrent, extraosseous multiple myeloma.
[electronic resource]
by
Peters, F
Cathomas, G
Rothen, M
Thurnheer, R
Rutishauser, J
Producer:
20030428
In:
Postgraduate medical journal
vol. 79
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9.
Growth hormone, but not insulin-like growth factor I, induces a serum protease activity for insulin-like growth factor binding protein-3 in hypophysectomized rats in vivo.
[electronic resource]
by
Rutishauser, J
Schmid, C
Hauri, C
Froesch, E R
Zapf, J
Producer:
19931213
In:
FEBS letters
vol. 334
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10.
Intact but not truncated insulin-like growth factor binding protein-3 (IGFBP-3) blocks IGF I-induced stimulation of osteoblasts: control of IGF signalling to bone cells by IGFBP-3-specific proteolysis?
[electronic resource]
by
Schmid, C
Rutishauser, J
Schläpfer, I
Froesch, E R
Zapf, J
Producer:
19911002
In:
Biochemical and biophysical research communications
vol. 179
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11.
[Subtherapeutic blood levels of phenytoin due to a medication error].
[electronic resource]
by
Burri, E
Rüegg, S
Rutishauser, J
Egger, S S
Lampert, M L
Producer:
20070524
In:
Praxis
vol. 96
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12.
A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus.
[electronic resource]
by
Rutishauser, J
Kopp, P
Gaskill, M B
Kotlar, T J
Robertson, G L
Producer:
19990706
In:
Molecular genetics and metabolism
vol. 67
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13.
Intravenously injected insulin-like growth factor (IGF) I/IGF binding protein-3 complex exerts insulin-like effects in hypophysectomized, but not in normal rats.
[electronic resource]
by
Zapf, J
Hauri, C
Futo, E
Hussain, M
Rutishauser, J
Maack, C A
Froesch, E R
Producer:
19950209
In:
The Journal of clinical investigation
vol. 95
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14.
A novel point mutation in the translation initiation codon of the pre-pro-vasopressin-neurophysin II gene: cosegregation with morphological abnormalities and clinical symptoms in autosomal dominant neurohypophyseal diabetes insipidus.
[electronic resource]
by
Rutishauser, J
Böni-Schnetzler, M
Böni, J
Wichmann, W
Huisman, T
Vallotton, M B
Froesch, E R
Producer:
19960220
In:
The Journal of clinical endocrinology and metabolism
vol. 81
Online resources:
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