Page last updated: 2024-08-22

magnesium sulfate and Genetic Predisposition

magnesium sulfate has been researched along with Genetic Predisposition in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	3 (75.00)	24.3611
2020's	1 (25.00)	2.80

Authors

Authors	Studies
Haak, P; Korzeniewski, SJ; Lenski, M; Paneth, N; Slaughter, J	1
Buhimschi, C; Caritis, SN; Carpenter, M; Costantine, MM; Dudley, DJ; Jablonski, KA; Leveno, KJ; Malone, FD; Mercer, BM; O'sullivan, MJ; Peaceman, AM; Ramin, SM; Reddy, UM; Rouse, DJ; Sorokin, Y; Thorp, JM; Varner, MW; Wapner, RJ	1
Clark, EA; Varner, M	1
Al-Harbi, H; Habeb, AM; Schlingmann, KP	1

Reviews

2 review(s) available for magnesium sulfate and Genetic Predisposition

Article	Year
The complex aetiology of cerebral palsy. Nature reviews. Neurology, 2018, Volume: 14, Issue:9 Topics: Anticonvulsants; Cerebral Palsy; Child; Congenital Abnormalities; Female; Genetic Predisposition to Disease; Humans; Hypothermia, Induced; Infant, Newborn; Infant, Premature, Diseases; Magnesium Sulfate; Pregnancy; Pregnancy Complications	2018
Impact of preterm PROM and its complications on long-term infant outcomes. Clinical obstetrics and gynecology, 2011, Volume: 54, Issue:2 Topics: Adrenal Cortex Hormones; Cytokines; Female; Fetal Membranes, Premature Rupture; Genetic Predisposition to Disease; Gestational Age; Humans; Infant, Newborn; Inflammation; Magnesium Sulfate; Nervous System Diseases; Pregnancy; Premature Birth; Prognosis; Time Factors; Tocolytic Agents	2011

Article

Year

The complex aetiology of cerebral palsy.

Nature reviews. Neurology, 2018, Volume: 14, Issue:9

Topics: Anticonvulsants; Cerebral Palsy; Child; Congenital Abnormalities; Female; Genetic Predisposition to Disease; Humans; Hypothermia, Induced; Infant, Newborn; Infant, Premature, Diseases; Magnesium Sulfate; Pregnancy; Pregnancy Complications

2018

Impact of preterm PROM and its complications on long-term infant outcomes.

Clinical obstetrics and gynecology, 2011, Volume: 54, Issue:2

Topics: Adrenal Cortex Hormones; Cytokines; Female; Fetal Membranes, Premature Rupture; Genetic Predisposition to Disease; Gestational Age; Humans; Infant, Newborn; Inflammation; Magnesium Sulfate; Nervous System Diseases; Pregnancy; Premature Birth; Prognosis; Time Factors; Tocolytic Agents

2011

Other Studies

2 other study(ies) available for magnesium sulfate and Genetic Predisposition

Article	Year
Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery. American journal of perinatology, 2020, Volume: 37, Issue:3 Topics: Case-Control Studies; Cerebral Palsy; Female; Genetic Predisposition to Disease; Humans; Infant; Interleukin-6; Logistic Models; Magnesium Sulfate; Male; Neurodevelopmental Disorders; Polymorphism, Single Nucleotide; Pregnancy; Premature Birth; Psychomotor Disorders; Sex Factors; Tocolytic Agents	2020
Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRPM6 gene mutation. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 2012, Volume: 23, Issue:5 Topics: Basal Ganglia Diseases; Biomarkers; Calcinosis; DNA Mutational Analysis; Female; Frameshift Mutation; Genetic Predisposition to Disease; Homozygote; Humans; Hypocalcemia; Infant; Magnesium; Magnesium Deficiency; Magnesium Sulfate; Phenotype; Renal Tubular Transport, Inborn Errors; Seizures; Tomography, X-Ray Computed; Treatment Outcome; TRPM Cation Channels	2012

Article

Year

Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery.

American journal of perinatology, 2020, Volume: 37, Issue:3

Topics: Case-Control Studies; Cerebral Palsy; Female; Genetic Predisposition to Disease; Humans; Infant; Interleukin-6; Logistic Models; Magnesium Sulfate; Male; Neurodevelopmental Disorders; Polymorphism, Single Nucleotide; Pregnancy; Premature Birth; Psychomotor Disorders; Sex Factors; Tocolytic Agents

2020

Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRPM6 gene mutation.

Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 2012, Volume: 23, Issue:5

Topics: Basal Ganglia Diseases; Biomarkers; Calcinosis; DNA Mutational Analysis; Female; Frameshift Mutation; Genetic Predisposition to Disease; Homozygote; Humans; Hypocalcemia; Infant; Magnesium; Magnesium Deficiency; Magnesium Sulfate; Phenotype; Renal Tubular Transport, Inborn Errors; Seizures; Tomography, X-Ray Computed; Treatment Outcome; TRPM Cation Channels

2012