Newborn Infant

NEONATAL SEIZURES DUE TO MATERNAL PRIMARY HYPERPARATHYROIDISM

Adolescent / Paediatrics / Pregnancy / Humans / Female / Male / Recurrence / Newborn Infant / Seizures / Hyperparathyroidism / Primary hyperparathyroidism / Male / Recurrence / Newborn Infant / Seizures / Hyperparathyroidism / Primary hyperparathyroidism

Paradoxical embolism in a preterm infant

Stroke / Humans / Male / Newborn Infant

Comentarios a la guía de práctica clínica de la ESC para el tratamiento de las enfermedades cardiovasculares durante el embarazo. Una visión crítica desde la cardiología española

Algorithms / Cardiology / Risk assessment / Lactation / Electrocardiography / Spain / Genetic counseling / Heart Failure / Pregnancy / Humans / Ischemia / Female / Advisory Committees / Myocardial Revascularization / Case Management / Anticoagulants / Risk factors / Newborn Infant / Acute Coronary Syndrome / Cardiac Arrhythmias / Adult / Prognosis / Cardiovascular Diseases / Risk Factors / Risk Assessment / Implantable defibrillators-cardioverters / Upper Extremity / Renal Artery / Mesenteric Arteries / Lower Extremity / Peripheral Arterial Disease / Thoracic Surgery / Primary Prevention / Spain / Genetic counseling / Heart Failure / Pregnancy / Humans / Ischemia / Female / Advisory Committees / Myocardial Revascularization / Case Management / Anticoagulants / Risk factors / Newborn Infant / Acute Coronary Syndrome / Cardiac Arrhythmias / Adult / Prognosis / Cardiovascular Diseases / Risk Factors / Risk Assessment / Implantable defibrillators-cardioverters / Upper Extremity / Renal Artery / Mesenteric Arteries / Lower Extremity / Peripheral Arterial Disease / Thoracic Surgery / Primary Prevention

Linking Antley–Bixler syndrome and congenital adrenal hyperplasia: A novel case of P450 oxidoreductase deficiency

Genetics / STEROIDS / Pregnancy / Humans / Mutation / Female / Male / Infant / Phenotype / Clinical Sciences / Newborn Infant / Synostosis / Adult / Deficiency / Genitalia / Deficit / Syndrome / Female / Male / Infant / Phenotype / Clinical Sciences / Newborn Infant / Synostosis / Adult / Deficiency / Genitalia / Deficit / Syndrome

Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

Endocrinology / Menstruation / Adolescent / STEROIDS / Biological Sciences / Humans / Puberty / Female / Clinical / Male / Androgens / Young Adult / Karyotyping / Phenotype / Clinical Sciences / Newborn Infant / Genitalia / Ovarian cysts / Ovary / Hormone Replacement Therapy / Biochemistry and cell biology / Cohort Studies / Humans / Puberty / Female / Clinical / Male / Androgens / Young Adult / Karyotyping / Phenotype / Clinical Sciences / Newborn Infant / Genitalia / Ovarian cysts / Ovary / Hormone Replacement Therapy / Biochemistry and cell biology / Cohort Studies

Congenital epigastric evisceration: a case report

Case Report / Humans / Male / Pediatric Surgery / Pediatric / Newborn Infant / Spectrum / Abdominal Wall Hernias / Gastroschisis / Congenital Defect / Newborn Infant / Spectrum / Abdominal Wall Hernias / Gastroschisis / Congenital Defect

Intra-Individual Consistency in the Quality of Neonatal General Movements

Neonatology / Video Analysis / Humans / Movement / Female / Male / Clinical Sciences / Newborn Infant / Observer Variation / Videotape Recording / Nervous System / Sensitivity and Specificity / Male / Clinical Sciences / Newborn Infant / Observer Variation / Videotape Recording / Nervous System / Sensitivity and Specificity

Fallo terapéutico por resistencia antibacteriana intra-tratamiento, a propósito de dos casos clínicos

Osteoarthritis / Humans / Child / Escherichia coli / Male / Microbial genetic and drug resistance / Urinary Tract Infections / Newborn Infant / Anti-Bacterial Agents / Klebsiella pneumoniae / Microbial genetic and drug resistance / Urinary Tract Infections / Newborn Infant / Anti-Bacterial Agents / Klebsiella pneumoniae

HDR (Hypoparathyroidism, Deafness, Renal dysplasia) syndrome associated to GATA3 gene duplication

Genetics / Molecular Biology / Humans / Kidney / Female / Clinical Genetics / Infant / Gene Duplication / Deafness / Clinical Sciences / Newborn Infant / Syndrome / Hypoparathyroidism / Clinical Genetics / Infant / Gene Duplication / Deafness / Clinical Sciences / Newborn Infant / Syndrome / Hypoparathyroidism

Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing

Genetics / Mitochondria / Gene expression / Energy Metabolism / Mitochondrial DNA / Humans / Liver / Male / Muscles / Infant / Electron Transport / Newborn Infant / Myocardium / Mitochondrion / Humans / Liver / Male / Muscles / Infant / Electron Transport / Newborn Infant / Myocardium / Mitochondrion

Cerebral Palsy after Neonatal Encephalopathy: How Much Is Preventable?

Cerebral Palsy / Quebec / Gestational diabetes / Pregnancy / Humans / Placenta / Female / Registries / Newborn Infant / Chorioamnionitis / Dystocia / Placenta / Female / Registries / Newborn Infant / Chorioamnionitis / Dystocia

Pregnancy and Neonatal Diabetes Outcomes in Remote Australia (PANDORA) study

Nursing / Research Design / Child Development / Anthropometry / Social Class / Birth Weight / Gestational diabetes / Pregnancy / Humans / Female / Infant / Northern Territory / Newborn Infant / Public health systems and services research / Breast feeding / Gestational Age / Glucose Tolerance Test / Pregnancy Outcome / Birth Weight / Gestational diabetes / Pregnancy / Humans / Female / Infant / Northern Territory / Newborn Infant / Public health systems and services research / Breast feeding / Gestational Age / Glucose Tolerance Test / Pregnancy Outcome

Spatiotemporal 16p11.2 Protein Network Implicates Cortical Late Mid-Fetal Brain Development and KCTD13-Cul3-RhoA Pathway in Psychiatric Diseases

Adolescent / Signal Transduction / Brain / Humans / Child / Young Adult / Infant / Mental Disorders / Neurons / Gene Regulatory Networks / Newborn Infant / Adult / Neuron / Fetus / Gene expression profiling / Young Adult / Infant / Mental Disorders / Neurons / Gene Regulatory Networks / Newborn Infant / Adult / Neuron / Fetus / Gene expression profiling

BCR-ABL rearrangement frequencies in chronic myeloid leukemia and acute lymphoblastic leukemia in Ecuador, South America

Ecuador / Adolescent / Cancer Genetics / Humans / Child / Female / Male / Infant / Karyotyping / Bone marrow / South America / Newborn Infant / Aged / Middle Aged / Chronic myeloid leukemia / Genotype / Adult / Ethnic Group / Acute Lymphoblastic Leukemia / Female / Male / Infant / Karyotyping / Bone marrow / South America / Newborn Infant / Aged / Middle Aged / Chronic myeloid leukemia / Genotype / Adult / Ethnic Group / Acute Lymphoblastic Leukemia

Human Coenzyme Q10 Deficiency

Genetics / Biological Sciences / Humans / Mutation / Infant / Newborn Infant / Coenzyme Q / Nervous System Diseases / Neurochemical / Newborn Infant / Coenzyme Q / Nervous System Diseases / Neurochemical

Isotropic apparent diffusion coefficient mapping of postnatal cerebral development

Brain Mapping / Prospective studies / Humans / Cerebral Cortex / Neuroradiology / Infant / Switzerland / Apparent Diffusion Coefficient / Clinical Sciences / Newborn Infant / White matter / Basal ganglia / Water Content / Reference Values / Neurosciences / Infant / Switzerland / Apparent Diffusion Coefficient / Clinical Sciences / Newborn Infant / White matter / Basal ganglia / Water Content / Reference Values / Neurosciences

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