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Juvenile hemochromatosis
Known as:
Hemochromatosis, type 2
, HEMOCHROMATOSIS, JUVENILE
, hemochromatosis juvenile
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National Institutes of Health
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Related topics
Related topics
4 relations
Narrower (1)
HEMOCHROMATOSIS, TYPE 2A
HFE2 gene
Broader (2)
Hemochromatosis
Iron Metabolism Disorders
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Determining the extent to which weather-related abiotic factors influence daily variation in early benthic phase mortality of intertidal marine invertebrates
Brittany T. Jenewein
2013
Corpus ID: 89904508
Populations of marine intertidal invertebrates vary substantially in abundance from year to year. These differences might be…
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2010
2010
Expression BMP 6-mediated Signaling and Gene and Inhibits both BMP 2-and Morphogenetic Protein ( BMP ) Antagonist c / Hemojuvelin Is a Broad Spectrum Bone Soluble Repulsive Guidance Molecule Signal…
M. Nili
,
U. Shinde
,
P. Rotwein
2010
Corpus ID: 205301386
2010
2010
Water / Fat resolved Whole-Heart Imaging for Coronary MRA
P. Koken
,
H. Eggers
,
G. Beck
,
P. Börnert
2010
Corpus ID: 29303186
Introduction Whole heart coronary MR-angiography methods (CMRA) utilizing parallel reception allow to image the entire 3D…
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2009
2009
A Simple Approach for Mapping CSF Volume Fraction
Q. Qin
,
P. V. Zijl
2009
Corpus ID: 27921486
INTRODUCTION: Cerebrospinal fluid (CSF) is important for the hydrodynamic function of the central nervous system. Although long…
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2006
2006
Het huisartsgeneeskundig handelen bij erectieproblemen – gegevens uit de Continue Morbiditeits Registratie Peilstations Nederland
H. Kedde
,
G. Donker
2006
Corpus ID: 72135703
SamenvattingKedde JH, Donker GA. Het huisartsgeneeskundig handelen bij erectieproblemen – gegevens uit de Continue Morbiditeits…
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2005
2005
Junge Patientin mit Diabetes mellitus, kleinknotiger Leberzirrhose, hoher Transferrin-Sättigung und negativem HFE-Test
M. Eisold
,
S. Gehrke
,
W. Stremmel
,
R. Gugler
2005
Corpus ID: 71278410
Anamnese: Eine 28-jahrige Patientin mit neu diagnostiziertem Diabetes mellitus, Hautpigmentierungen, Hepato- und Splenomegalie…
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2004
2004
To the editor : Homozygosity for a novel nonsense mutation ( G 66 X ) of the HJV gene causes severe juvenile hemochromatosis with fatal cardiomyopathy
A. Jánosi
,
H. Andrikovics
,
+4 authors
A. Tordai
2004
Corpus ID: 42243548
Juvenile hemochromatosis (JH) is a rare autosomal recessive disorder of iron metabolism. The early onset of severe iron overload…
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2001
2001
Evaluation of Brain Atrophy Measurements from Multiple Scanners
E. Fisher
,
K. Dixon
,
D. Finelli
,
Jean A. Tkach
,
F. Difilippo
2001
Corpus ID: 74137367
Introduction Whole brain atrophy has been proposed as a marker of disease progression in a number of neurological diseases…
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Review
1993
Review
1993
Review of Automatic Control of Aircraft and Missiles by Blakelock JH
D. Cowling
1993
Corpus ID: 114574694
1981
1981
Dual effect of carbonic anhydrase inhibitors on H+ transport by the turtle bladder.
L. Norby
,
D. Bethencourt
,
J. Schwartz
American Journal of Physiology
1981
Corpus ID: 25218280
Previous studies in isolated turtle bladder have demonstrated that high concentrations of carbonic anhydrase (CA) inhibitors…
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