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Neurofibromatosis -- Treatment : Multidisciplinary approach to neurofibromatosis type 1 / Gianluca Tadini, Eric Legius, Hilde Brems, editors  2020 1
 

Neurofibromatosis Type 1 -- See Neurofibromatosis 1


An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS)
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Neurofibromatosis Type 3 -- See Neurofibromatoses


A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
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Neurofibromatosis Type 3s -- See Neurofibromatoses


A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
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Neurofibromatosis Type I -- See Neurofibromatosis 1


An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS)
  1
 

Neurofibromin 1 -- See Also Neurofibromatosis 1


An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS)
  1
 

Neurofibromin 2 -- See Also Genes, Neurofibromatosis 2


Tumor suppressor genes located on the long arm of human chromosome 22. Mutation or loss of these genes causes NEUROFIBROMATOSIS 2
  1
 

Neurofilaments -- See Cytoplasmic filaments


  1
Neurofilosofi. : The Cambridge handbook of consciousness / edited by Philip David Zelazo, Morris Moscovitch, Evan Thompson  2007 1
Neurofisiologia.   14
Neurofysiologi.   2
Neurofysiologie.   14
Neurogenese   2
 

Neurogeneses -- See Neurogenesis


Formation of NEURONS which involves the differentiation and division of STEM CELLS in which one or both of the daughter cells become neurons
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Neurogenesis -- See Developmental neurobiology


Here are entered works on the growth and differentiation of the nervous system. Works limited to the growth of the nervous system are entered under Nervous system--Growth
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Neurogenesis   13
 

Neurogenesis, Bladder -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
Neurogenesis -- physiology : Adult neurogenesis in the hippocampus : health, psychopathology, and brain disease / edited by Juan J. Canales  2016 1
 

Neurogenesis, Urinary Bladder -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
Neurogenetics   51
Neurogenetics -- Animal models : What's wrong with my mouse? : behavioral phenotyping of transgenic and knockout mice / Jacqueline N. Crawley  2007 1
Neurogenetics -- Computer simulation   3
Neurogenetics -- Congresses. : Neurons, circuitry, and plasticity in the spinal cord and brainstem / issue editors, Lea Ziskind-Conhaim, Amy B. McDermott, Francisco J. Alvarez, John D. Houle, and Shawn Hochman    1
Neurogenetics -- Laboratory manuals   2
Neurogenetics -- Mathematical models : Computational neurogenetic modeling / Lubica Benuskova and Nikola Kasabov  2007 1
Neurogenetics -- Methodology : Methods in genomic neuroscience / edited by Hemin R. Chin, Steven O. Moldin  2001 1
Neurogenetics -- Periodicals   5
Neurogenetics -- Research -- Methodology   2
Neurogenetik   3
 

Neurogenic Acroosteolyses -- See Hereditary Sensory and Autonomic Neuropathies


A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
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Neurogenic Acroosteolysis -- See Hereditary Sensory and Autonomic Neuropathies


A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
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Neurogenic Bladder -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
Neurogenic bladder.   6
 

Neurogenic Bladder, Atonic -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
 

Neurogenic Bladder Disorder -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
 

Neurogenic Bladder Disorders -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
Neurogenic bladder -- Periodicals : International neurourology journal (Online)    1
 

Neurogenic Bladder, Spastic -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
Neurogenic bladder -- Treatment : Pediatric urinary bladder tissue engineering / Arun K. Sharma and Earl Y. Cheng  2012 1
 

Neurogenic Bladder, Uninhibited -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
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Neurogenic Bowels -- See Neurogenic Bowel


Loss or absence of normal intestinal function due to nerve damage or birth defects. It is characterized by the inability to control the elimination of stool from the body
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Neurogenic Communication Disorder -- See Communication Disorders


Disorders of verbal and nonverbal communication caused by receptive or expressive LANGUAGE DISORDERS, cognitive dysfunction (e.g., MENTAL RETARDATION), psychiatric conditions, and HEARING DISORDERS
  1
 

Neurogenic Communication Disorders -- See Communication Disorders


Disorders of verbal and nonverbal communication caused by receptive or expressive LANGUAGE DISORDERS, cognitive dysfunction (e.g., MENTAL RETARDATION), psychiatric conditions, and HEARING DISORDERS
  1
 

Neurogenic Dysfunction of the Urinary Bladder -- See Urinary Bladder, Neurogenic


Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES
  1
 

Neurogenic Inflammation -- See Also Neuroimmunomodulation


The biochemical and electrophysiological interactions between the NERVOUS SYSTEM and IMMUNE SYSTEM
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Neurogenic Inflammation   4
Neurogenic Inflammation -- physiopathology : Multiple Sclerosis and CNS Inflammatory Disorders  2014 1
 

Neurogenic Inflammations -- See Neurogenic Inflammation


Inflammation caused by an injurious stimulus of peripheral neurons and resulting in release of neuropeptides which affect vascular permeability and help initiate proinflammatory and immune reactions at the site of injury
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Neurogenic Muscular Atrophies -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
  1
 

Neurogenic Muscular Atrophy -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
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