X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (338) 338
magnesium (215) 215
female (214) 214
index medicus (210) 210
male (148) 148
magnesium - blood (101) 101
pregnancy (91) 91
adult (90) 90
calcium (79) 79
animals (78) 78
infant, newborn (65) 65
pediatrics (62) 62
infant (58) 58
child (56) 56
hypomagnesemia (53) 53
middle aged (48) 48
magnesium deficiency - complications (45) 45
mutation (45) 45
adolescent (43) 43
calcium - blood (42) 42
magnesium - metabolism (42) 42
research (42) 42
endocrinology & metabolism (39) 39
health aspects (38) 38
metabolism (37) 37
risk factors (37) 37
zinc (37) 37
biochemistry & molecular biology (36) 36
child, preschool (35) 35
aged (33) 33
magnesium deficiency - blood (33) 33
magnesium deficiency - congenital (33) 33
medicine & public health (33) 33
magnesium deficiency - diagnosis (32) 32
analysis (31) 31
children (31) 31
nutrition (31) 31
magnesium - therapeutic use (30) 30
urology & nephrology (29) 29
care and treatment (28) 28
infants (26) 26
life sciences (26) 26
trace elements (26) 26
dietary supplements (25) 25
magnesium deficiency - genetics (25) 25
nutrition & dietetics (25) 25
oncology (25) 25
diet (24) 24
disease (24) 24
hypocalcemia (24) 24
medicine (24) 24
risk (24) 24
women (24) 24
biochemistry, general (23) 23
deficiency (23) 23
magnesium deficiency - etiology (23) 23
physiological aspects (23) 23
prospective studies (23) 23
proteins (23) 23
selenium (23) 23
magnesium - administration & dosage (22) 22
copper (21) 21
nephrology (21) 21
young adult (21) 21
calcium - metabolism (20) 20
patients (20) 20
pregnant women (20) 20
rats (20) 20
review (20) 20
diabetes (19) 19
magnesium deficiency diseases (19) 19
potassium (19) 19
prevalence (19) 19
familial hypomagnesemia (18) 18
magnesium-sulfate (18) 18
multidisciplinary sciences (18) 18
obstetrics & gynecology (18) 18
biotechnology (17) 17
calcium - urine (17) 17
clinical neurology (17) 17
homeostasis (17) 17
hypertension (17) 17
hypocalcemia - etiology (17) 17
iron (17) 17
magnesium deficiency - drug therapy (17) 17
physiology (17) 17
preeclampsia (17) 17
serum (17) 17
sodium (17) 17
cardiac & cardiovascular systems (16) 16
diagnosis (16) 16
magnesium sulfate (16) 16
magnesium-deficiency (16) 16
medical research (16) 16
mortality (16) 16
genes (15) 15
genetic aspects (15) 15
internal medicine (15) 15
magnesium deficiency - physiopathology (15) 15
mutations (15) 15
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (466) 466
French (9) 9
German (2) 2
Chinese (1) 1
Danish (1) 1
Dutch (1) 1
Greek (1) 1
Polish (1) 1
Spanish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


International journal of molecular sciences, ISSN 1422-0067, 2019, Volume 20, Issue 17, p. 4164
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 04/2012, Volume 105, Issue 4, pp. 634 - 641
Journal Article
Current opinion in nephrology and hypertension, ISSN 1062-4821, 2016, Volume 25, Issue 4, pp. 301 - 307
PURPOSE OF REVIEWIdentification of the mechanisms of magnesium absorption and reabsorption has markedly enhanced our understanding of the causes of... 
TRPM6/7 | hypomagnesemia | hereditary causes of hypomagnesemia | proton pump inhibitors | epidermal growth factor | FAMILIAL HYPOMAGNESEMIA | DISORDERS | MAGNESIUM | HYPERCALCIURIA | TRANSPORT | CLDN19 | UROLOGY & NEPHROLOGY | PERIPHERAL VASCULAR DISEASE | MUTATIONS | KIDNEY | TRPM6 | EXPRESSION | Hypocalcemia - metabolism | Humans | Sodium Potassium Chloride Symporter Inhibitors - adverse effects | Water-Electrolyte Imbalance - etiology | Intestines - metabolism | Pancreatitis - complications | Nephrocalcinosis - complications | Magnesium Deficiency - complications | Nephrocalcinosis - metabolism | Renal Tubular Transport, Inborn Errors - metabolism | Bartter Syndrome - metabolism | Hypocalcemia - complications | Intestinal Elimination | Proton Pump Inhibitors - adverse effects | Hypoparathyroidism - congenital | Magnesium Deficiency - congenital | Water-Electrolyte Imbalance - chemically induced | Bartter Syndrome - complications | Magnesium - metabolism | Renal Tubular Transport, Inborn Errors - complications | Magnesium Deficiency - metabolism | Hypoparathyroidism - metabolism | Renal Elimination | Hypercalciuria - complications | Water-Electrolyte Imbalance - metabolism | Hypercalciuria - metabolism | Gitelman Syndrome - complications | Hypoparathyroidism - complications | Gitelman Syndrome - metabolism | Pancreatitis - metabolism | Nephrons - metabolism
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 08/2016, Volume 24, Issue 9, pp. 1274 - 1279
... marriage featuring a novel combination of congenital hypothyroidism, hypomagnesemia and hypercholesterolemia... 
EXOME | SECONDARY HYPOCALCEMIA | FAMILIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | DISORDERS | MUTATIONS | TRPM6 | THYROGLOBULIN GENE | DISCOVERY | GENOME | HYPOMAGNESEMIA | Intestinal Diseases - complications | Lipid Metabolism, Inborn Errors - genetics | Lipoproteins - genetics | Humans | Hypothyroidism - complications | Male | Magnesium Deficiency - diagnosis | Young Adult | Magnesium Deficiency - genetics | Magnesium Deficiency - complications | RNA Splicing | Female | Hypothyroidism - genetics | Phytosterols - adverse effects | Lipid Metabolism, Inborn Errors - diagnosis | Intestinal Diseases - genetics | Hypothyroidism - diagnosis | Phytosterols - genetics | Intestinal Diseases - diagnosis | Phenotype | Pedigree | Adolescent | Hypercholesterolemia - diagnosis | Thyroglobulin - genetics | TRPM Cation Channels - genetics | Hypercholesterolemia - complications | Consanguinity | Hypercholesterolemia - genetics | Lipid Metabolism, Inborn Errors - complications | Mutation | ATP Binding Cassette Transporter, Sub-Family G, Member 5 - genetics | Alternative splicing | Pediatrics | Phenotypes | Congenital diseases | Internal medicine | Genomes | Thyroid gland | Sitosterolemia | Hypothyroidism | Patients | Medicine | Transient receptor potential proteins | Hypercholesterolemia | Sterols | Thyroglobulin | Atherosclerosis | Genetics | Magnesium | Diagnosis | Bioinformatics | Hypomagnesemia | Genotypes
Journal Article
Digestive diseases and sciences, ISSN 1573-2568, 2011, Volume 56, Issue 4, pp. 931 - 950
... that have generated the greatest concern: B12 deficiency; iron deficiency; hypomagnesemia; increased susceptibility to pneumonia, enteric infections, and fractures... 
Biochemistry, general | Oncology | Infections | Adverse effects | Transplant Surgery | Fractures | Medicine & Public Health | Hepatology | Gastroenterology | Proton pump inhibitors | Malabsorption | Safety | Interactions | Cancer | CLOSTRIDIUM-DIFFICILE INFECTION | COMMUNITY-ACQUIRED PNEUMONIA | BONE-MINERAL DENSITY | ZOLLINGER-ELLISON-SYNDROME | HELICOBACTER-PYLORI INFECTION | GASTROESOPHAGEAL-REFLUX DISEASE | GASTRIC ENDOCRINE-CELLS | FUNDIC GLAND POLYPS | FAMILIAL ADENOMATOUS POLYPOSIS | ACID-SUPPRESSIVE THERAPY | GASTROENTEROLOGY & HEPATOLOGY | Pneumonia - physiopathology | Diarrhea - physiopathology | Humans | Congenital Abnormalities - etiology | Congenital Abnormalities - physiopathology | Stomach Diseases - chemically induced | Male | Diarrhea - chemically induced | Stomach Neoplasms - physiopathology | Drug Interactions | Vitamin B 12 Deficiency - chemically induced | Iron - deficiency | Stomach Diseases - physiopathology | Female | Anti-Ulcer Agents - therapeutic use | Proton Pump Inhibitors - adverse effects | Pneumonia - etiology | Carcinoid Tumor - chemically induced | Anti-Ulcer Agents - adverse effects | Rats | Treatment Outcome | Vitamin B 12 Deficiency - physiopathology | Proton Pump Inhibitors - therapeutic use | Carcinoid Tumor - physiopathology | Animals | Fractures, Bone - physiopathology | Stomach Neoplasms - chemically induced | Fractures, Bone - chemically induced | Magnesium - blood | Osteoporosis | Complications and side effects | Medical colleges | Pneumonia | Care and treatment | Bacterial pneumonia | Birth defects | Disease susceptibility | Risk factors
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 2014, Volume 22, Issue 4, pp. 497 - 504
Journal Article
BMJ case reports, ISSN 1757-790X, 09/2016, Volume 2016, p. bcr2016216870
Magnesium is the second most abundant intracellular cation and plays an essential role in neuronal, skeletal and cardiac tissue. Hypomagnesaemia can cause... 
Epilepsy, Tonic-Clonic - genetics | Hypocalcemia - complications | Magnesium Deficiency - genetics | Magnesium Deficiency - complications | Magnesium Deficiency - congenital | Humans | Hypocalcemia - genetics | TRPM Cation Channels - genetics | Female | Mutation | Infant, Newborn
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 2017, Volume 58, Issue 12, pp. 2348 - 2364
Lipin-1 is a Mg2+-dependent phosphatidic acid phosphatase (PAP) that in mice is necessary for normal glycerolipid biosynthesis, controlling adipocyte... 
Lipodystrophies | Inborn errors of metabolism | Human fat lipid analysis | Human lipids | Adipogenic differentiation | Adipocytes | Gene expression | Phosphatases/lipid | MACROPHAGE INFILTRATION | inborn errors of metabolism | phosphatases/lipid | adipogenic differentiation | human fat lipid analysis | FAMILIAL PARTIAL LIPODYSTROPHY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHOSPHATIDATE PHOSPHATASES | human lipids | lipodystrophies | SKELETAL-MUSCLE | ACTIVATED-RECEPTOR-GAMMA | GENE-EXPRESSION | CONGENITAL GENERALIZED LIPODYSTROPHY | MESENCHYMAL-STEM-CELLS | LIPIN 1 | TRIGLYCERIDE SYNTHESIS | adipocytes | gene expression | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | Body Weight | Humans | Middle Aged | Adipose Tissue, White - metabolism | Child, Preschool | Adipocytes - cytology | Male | Phosphatidate Phosphatase - genetics | PPAR gamma - metabolism | Case-Control Studies | Phosphatidate Phosphatase - deficiency | Adipose Tissue, White - cytology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism | Rhabdomyolysis - pathology | Female | Cell Differentiation | Body Fat Distribution | Child | Sterol Regulatory Element Binding Protein 1 - metabolism | PPAR gamma - genetics | Gene Expression Regulation | Rhabdomyolysis - metabolism | Sterol Regulatory Element Binding Protein 1 - genetics | Rhabdomyolysis - genetics | Adipocytes - metabolism | Adolescent | Alleles | Mutation | Adipose tissue | Mesenchyme | Lipids | Rhabdomyolysis | Lipodystrophy | Lpin1 gene | Peroxisome proliferator-activated receptors | Magnesium | Acid phosphatase | Phosphatidic acid | Life Sciences | Patient-Oriented and Epidemiological Research | lipid | phosphatases
Journal Article
Trace Elements and Electrolytes, ISSN 0946-2104, 2011, Volume 28, Issue 4, pp. 232 - 241
Magnesium deficiency tetany (MDT) is a separate hereditary illness. It occurs more often than is assumed or even diagnosed today... 
Magnesium deficiency | Therapy | Genetics | Metabolism | Tetany | genetics | magnesium deficiency | therapy | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | ENDOCRINOLOGY & METABOLISM | metabolism | TRPM6 | tetany | HYPOMAGNESEMIA
Journal Article
ARCHIVES DE PEDIATRIE, ISSN 0929-693X, 11/2013, Volume 20, Issue 11, pp. 1212 - 1218