700 Journals and 15,000,000 Readers
Each Journal is getting 25,000+ Readers
Journal of Pediatric Neurology and Medicine is a peer reviewed journal that caters to the needs of scientific community by publishing innovations, discoveries and the latest advancements in the field.
This journal offers an open access platform for the authors to contribute their research on different aspects of Hospitality and Clinical pharmacy by publishing complete and reliable source of information as Research articles, review articles, short communications, editorials, case reports, and letters to the editor.
Journal of Pediatric Neurology and Medicine seeks high quality submissions and welcomes contributions in aspects like Epilepsy, Mitochondrial diseases, Congenital malformations, Chromosomopathies, Peripheral neuropathies, Perinatal, Childhood stroke, Cerebral palsy and Children with neurological disease.
The journal is using Editorial Tracking System for online manuscript submission, review and tracking. Submit manuscript at http://www.editorialmanager.com/medicaljournals/ or send as an e-mail attachment to the Editorial Office at
Mitochondrial maladies result from disappointments of the mitochondria, specific compartments display in every cell of the body with the exception of red platelets. Mitochondria are in charge of making more than ninety per cent of the vitality required by the body to manage life and bolster development. When they come up short, less and less vitality is created inside of the cell. Cell harm and even cell demise take after. In the event that this procedure is rehashed all through the body, entire frameworks start to fizzle, and the life of the individual in whom this is going on is seriously traded off. The infection principally influences youngsters, however grown-up onset is turning out to be more normal. Infections of the mitochondria seem to bring about the most harm to cells of the cerebrum, heart, liver, skeletal muscles, kidney and the endocrine and respiratory frameworks
Related Journals of Mitochondrial disease
Clinical & Medical Biochemistry: Open Access, Biochemistry & Physiology: Open Access, Biomolecular Research & Therapeutics, Journal of Molecular and Genetic Medicine, Mitochondrion, Mitochondrial Disease, Primer on mitochondrial disease, Genetics of mitochondrial diseases, The “new” mitochondrial disorders, Monogenic Mitochondrial Disorders, Pediatric Neurology, Neurology.
Congenital abnormalities from the norm, called contortions, are conditions that are available during childbirth (intrinsic). There are various varieties of innate deformities of the bone and delicate tissue of the head and spine, including neural tube deserts, for example, spina bifida. Some inherent mutations are mellow and some are extreme however correctable with surgery by a pediatric neurosurgeon.
Related Journals of Congenital malformation
Anaplastology, Human Genetics & Embryology, Journal of Neonatal Biology, Congenital Heart Disease, Congenital Anomalies, World Journal for Pediatric and Congenital Heart Surgery, Journal of Pediatrics, Congenital Disorders, Pediatric Research, Journal of Perinatology.
Peripheral nervous system connects the nerves from the brain and spinal cord (central nervous system) to the rest of the body, including the arms, hands, feet, legs, internal organs, mouth and face. The job of these nerves is to deliver signals about physical sensations back to your brain. Peripheral neuropathy is a disorder that occurs when these nerves malfunction because they are damaged or destroyed. This disrupts the nerves’ normal functioning. They might send signals of pain when there is nothing causing pain, or they might not send a pain signal even if something is harming you. This can be caused by injury, systemic illness, infection, or may be associated with an inherited disorder.
Related Journals of Peripheral Neuropathy
International Journal of Physical Medicine & Rehabilitation, Journal of Neuroinfectious Diseases, Hereditary Genetics: Current Research, Diabetic Neuropathies, Journal of Neuropathology & Experimental Neurology, The Neuropathy Journal, BMC Pediatrics, Italian Journal of Pediatrics, Pediatrics.
Fringe sensory system join the nerves from the cerebrum and spinal line (focal sensory system) to whatever is left of the body, including the arms, hands, feet, legs, inside organs, mouth and face. The occupation of these nerves is to convey motions about physical sensations back to your mind. Fringe neuropathy is an issue that happens when these nerves glitch on the grounds that they are harmed or wrecked. This upsets the nerves' typical working. They may send signs of agony when there is nothing bringing on torment, or they may not send a torment flag regardless of the fact that something is hurting you. This can be created by damage, systemic ailment, contamination, or may be connected with an acquired issue.
Related Journals of Childhood Stroke
Journal of Neurology & Neurophysiology, Journal of Neurological Disorders, International Journal of Neurorehabilitation, Journal of Stroke and Cerebrovascular Diseases, International Journal of Stroke, Stroke, Stroke Research and Treatment, International Journal of Emergency Medicine, JAMA Pediatrics, Child and Adolescent Psychiatry and Mental Health.
Neuromuscular sicknesses are a main reason for handicap in youngsters and much of the time result from hereditary anomalies that change the structure and capacity of muscles and nerves. Late advances have prompted the revelations of hereditary deformities that cause a few neuromuscular maladies, including those that influence muscle (e.g. solid dystrophy, intrinsic myopathy); neuromuscular intersection (e.g. inborn myasthesia disorders); and nerves (e.g. acquired neuropathies and spinal strong decays).
Related Journals of Children with neurological disease
Pertaining to the period immediately before and after birth. The perinatal period is defined in diverse ways. Depending on the definition, it starts at the 20th to 28th week of gestation and ends 1 to 4 weeks after birth.
Related Journals of Perinatal
Pre-birth hereditary determination administrations incorporate numerical and basic chromosomal variations from the norm, monogenic infections and metabolic issue. The demonstrative systems utilized cytogenetic methods of atomic cyto genetics and sub-atomic examination of DNA.
Related Journals of Chromosomopathy