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         Neurofibromatosis:     more books (99)
  1. Cafe Au Lait Spots May Signal Neurofibromatosis.(Brief Article): An article from: Family Practice News by Nancy Walsh, 2001-03-15
  2. Neurofibromatosis: a young woman's journey--case study.(Case study): An article from: Journal of Neuroscience Nursing by Susan Milliken, 2007-12-01
  3. Tuberous Sclerosis and Neurofibromatosis: Epidemiology, Pathophysiology, Biology, and Management : Proceedings of the International Symposium on Neu (Japan ... Foundation Publishing Series, No. 28) by International Symposium on Neurocutaneous Syndrome, Yasumasa Ishibashi, et all 1990-12
  4. Understanding neurofibromatosis: An introduction for patients and parents by James H Tonsgard, 1993
  5. Neurofibromatosis: January 1984 through June 1987, 720 citations (Literature search) by Jacqueline Van de Kamp, 1987
  6. Joint Resolution Designating November 1992 as "Neurofibromatosis Awareness Month." (SuDoc AE 2.110:102-577) by U.S. National Archives and Records Administration, 1992
  7. Neurofibromatosis Type I: From Genotype to Phenotype (A Volume in the Human Molecular Genetics Series) (Human Molecular Genetics) by M. Upadhyaya, 1980
  8. Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1 (The James A. Bush memorial research awards) by D. A Stevenson, 1997
  9. Descriptive analysis of tibal pseudarthrosis in patients with neurofibromatosis 1 (The James A. Bush Memorial Research Awards) by David A Stevenson, 1997
  10. Neurofibromatosis (Current problems in surgery) by John V Wander, 1977
  11. Fibroma molluscum, or universal neurofibromatosis by A Ravogli, 1911
  12. Neurofibromatosis (v. Recklinghausen's disease): A clinical -psychiatric and genetic study by Birgitta Samuelsson, 1981
  13. Type 1 neurofibromatosis and the pediatric patient (Current problems in pediatrics) by Vincent M Riccardi, 1992
  14. Las neurofibromatosis (SuDoc HE 20.3520:N 39/SPAN.) by U.S. Dept of Health and Human Services, 2000

61. Neurofibromatosis: What Is It?
Your Genes, Your Health, DNA Learning Center s multimedia guide to genetic, inherited disorders neurofibromatosis, NF, autosomal dominant,
http://www.ygyh.org/nf/whatisit.htm

Concept 1
: Children resemble their parents. Learn how Mendel worked out inheritance in pea plants.
Concept 10
: Chromosomes carry genes. Find out how genes are arranged on chromosomes.
Concept 27
: Mutations are changes in genetic information. Find out how mutations affect gene expression.

62. Neurofibromatosis - Genetics Home Reference
neurofibromatosis is a condition in which noncancerous tumors called neurofibromas The two main types of neurofibromatosis can be distinguished by the
http://ghr.nlm.nih.gov/condition=neurofibromatosis
Home What's New Browse Handbook ... Search Neurofibromatosis
Neurofibromatosis
On this page:
What is neurofibromatosis?
Neurofibromatosis is a condition in which noncancerous tumors called neurofibromas grow along nerves in the skin, brain, and other parts of the body. The two main types of neurofibromatosis can be distinguished by the locations of the tumors and by genetic testing. Genetic changes are related to the following types of neurofibromatosis. The features of neurofibromatosis depend on where the tumors are located and differ for each type of the condition. Sometimes the signs and symptoms are so mild that individuals may be unaware of having this disorder. In other cases, signs and symptoms can be very serious or life-threatening. For a discussion of specific features, please refer to the summaries for neurofibromatosis 1 and neurofibromatosis 2.
How common is neurofibromatosis?

63. Neurofibromatosis 1 - Genetics Home Reference
Where can I find additional information about neurofibromatosis 1? neurofibromatosis 1 is a condition in which noncancerous tumors called neurofibromas
http://ghr.nlm.nih.gov/condition=neurofibromatosis1
Home What's New Browse Handbook ... Search Neurofibromatosis 1
Neurofibromatosis 1
On this page:
What is neurofibromatosis 1?
Neurofibromatosis 1 is a condition in which noncancerous tumors called neurofibromas grow along nerves in the skin, brain, and other parts of the body. Neurofibromatosis 1 is a subtype of neurofibromatosis During childhood, benign (noncancerous) growths called Lisch nodules often appear in the iris (the colored part of the eye). Lisch nodules do not interfere with vision. Another type of tumor, called an optic glioma, can occur on the nerve leading from the eye to the brain and sometimes causes decreased vision or total vision loss. Additional signs and symptoms include high blood pressure and bony changes such as curvature of the spine (scoliosis). Most people with neurofibromatosis 1 have normal intelligence. Fewer than 10 percent are mentally retarded, but about half of affected children have learning disabilities.

64. Neurofibromatosis (NF1, NF2). DermNet NZ
Authoritative facts about the skin from the New Zealand Dermatological Society.
http://dermnetnz.org/systemic/neurofibromatosis.html
@import url("/common/screen.css");
DermNet NZ
Ad
Authoritative facts
about the skin from the New Zealand Dermatological Society Incorporated Home For patients For doctors ... Site map Search:
Home
Systemic
Neurofibromatosis
What is neurofibromatosis?
Neurofibromatosis (NF) is a genetic disorder that affects the bone, soft tissue, skin and nervous system. It is classified into 2 distinct types, neurofibromatosis 1 (NF1) and neurofibromatosis 2 (NF2). NF1 occurs in about 1 in 3000 births whilst NF2 only occurs in about 1 in 50,000 births. NF1, also known as von Recklinghausen disease, is characterised by the presence of:
  • 6 or more (defined oval-shaped light brown patches greater than 0.5cm in diameter) Multiple neurofibromas (tumours on, under, or hanging off the skin) Freckling (under the armpits and areas of skin folds such as the groin) Lisch nodules (tiny tumours on the iris of the eye)
NF2, also known as bilateral acoustic neurofibromatosis, is characterised by multiple tumours and lesions on the brain and spinal cord. Tumours growing on the auditory nerves that lead to hearing loss is usually the first symptom of the disease. Often this is not apparent until the late teens or early 20's.
What causes neurofibromatosis?

65. Neurofibromatosis
a CHORUS notecard document about neurofibromatosis.
http://chorus.rad.mcw.edu/doc/00722.html
CHORUS Collaborative Hypertext of Radiology Multisystem entities About CHORUS
Search

Feedback
neurofibromatosis
Charles E. Kahn, Jr., MD - 2 February 1995
Last updated 26 May 2004
Related CHORUS documents:
cafe-au-lait spots optic nerve glioma McCune-Albright syndrome harlequin eye ... phakomatoses
Search for related articles:
AJR American Journal of Roentgenology PubMed : index to biomedical literature ...

Medical College of Wisconsin

66. Neurofibromatosis - 1
neurofibromatosis (von Recklinghausen s Disease) - Back - Cafe au lait macules and neurofibromas. Return to Image Index page.
http://tray.dermatology.uiowa.edu/NF-001.htm
Dept. of Dermatology - University of Iowa College of Medicine
Neurofibromatosis - (von Recklinghausen's Disease) - Back - Cafe au lait macules and neurofibromas
Return to Image Index page. Return to Image Index page.
Return to Dermatology's Home page.
August, 1996

67. Neurofibromatosis - 2
neurofibromatosis (von Recklinghausen s Disease) - Low Back - Cafe au lait macule and neurofibroma. Return to Image Index page.
http://tray.dermatology.uiowa.edu/NF-002.htm
Dept. of Dermatology - University of Iowa College of Medicine
Neurofibromatosis - (von Recklinghausen's Disease) - Low Back - Cafe au lait macule and neurofibroma
Return to Image Index page. Return to Image Index page.
Return to Dermatology's Home page.
August, 1996

68. Neurofibrmatosis - Neurologychannel
neurofibromatosis is a genetic disorder that primarily affects nervous system function, neural cell growth, and the skin.
http://www.neurologychannel.com/neurofibromatosis/
Home Search SiteMap Ask the Dr. ... Medical Store
NEUROFIBROMATOSIS
Overview

Causes

Symptoms

Diagnosis
...
Prognosis
CONDITIONS
ADHD

ALS

Alzheimer's Disease

Autism
... Carpal Tunnel Syndrome Cephalic Disorders Cerebral Palsy Charcot-Marie-Tooth Disease Chronic Pain Dementia Encephalitis Epilepsy ... Guillain-Barre Syndrome Headache Huntington's Disease Hydrocephalus Lou Gehrig's Disease ... Traumatic Brain Injury Vertigo DIAGNOSTIC TESTS CT Scan MRI Scan TREATMENT OPTIONS
Botulinum Toxin Therapy Epidural Injection Trigger Point Injection Vagus Nerve Stimulation RESOURCES Clinical Trials Glossary Links MDLocator ... What Is a Neurologist? Videos FOR DOCTORS ONLY Website Services Get Listed in MDLocator CME ABOUT US Healthcommunities.com Testimonials print this email this Overview Neurofibromatosis (NF) is a genetic neurological disorder that affects cell growth in nerve tissue. NF produces tumors of the skin, internal organs, and nerves that may become cancerous (malignant). It also can affect bones, causing severe pain and debilitation and may result in learning disabilities, behavioral dysfunction, and hearing and vision loss. There is no cure for neurofibromatosis. Types Neurofibromatosis can be inherited as an autosomal dominant trait (a parent with the disorder has a 50% chance of passing it to an offspring) or can result from a spontaneous genetic mutation.

69. Biblioteca De Salud: Neurofibromatosis
neurofibromatosis Through Research
http://www.nacersano.org/centro/9388_9979.asp
9 de septiembre de 2005
Antes de Quedar Embarazada

Durante su Embarazo

Complicaciones

El Parto
...
Las Familias en la NICU

Biblioteca de Salud
Neurofibromatosis
  • Antecedentes familiares de NF1 en un padre, hermano o hijo.

The Children's Tumor Foundation: Ending Neurofibromatosis Through Research

95 Pine St., 16th Floor New York, NY 10005 (212) 344-6633 o (800)323-7938 Neurofibromatosis, Inc. 8855 Annapolis Rd., Suite 110 Lanham, MD 20706-2924 (301) 461-5213 (TDD) Referencias National Neurofibromatosis Foundation. What is NF? New York, N.Y., National Neurofibromatosis Foundation, 2000. Biblioteca de Salud Embarazo Ácido Fólico El Bajo Peso al Nacer El Embarazo Después de los 35 Años El Embarazo en las Adolescentes ... Un Buen Estado Físico para los Dos Infecciones/Enfermedades Durante el Embarazo Anormalidades del Líquido Amniótico Condiciones de la Placenta El VIH y el SIDA en el Embarazo Herpes Genital ... Trastornos Hepáticos durante el Embarazo Pruebas Diagnósticas Amniocentesis Análisis de la Sangre Materna Muestra del Villus Coriónico (CVS) Ultrasonido Alcohol, Drogas y Medicamentos Durante el Embarazo Accutane El Consumo de Alcohol Durante el Embarazo El consumo de drogas ílicitas durante el embarazo El Fumar Durante el Embarazo ... Talidomida Pérdida del Embarazo Aborto Espontáneo Embarazos Ectópicos y Molares Muerte del Feto Muerte del Neonato Defectos de Nacimiento y Condiciones Genéticas Acondroplasia Anemia Falciforme Anomalías Cromosómicas Defectos Cardíacos Congénitos ... Talasemia Para Recién Nacidos Diagnóstico Temprano para Recién Nacidos La Ictericia Neonatal La Lactancia Polio

70. Neurofibromatosis
Penn State Children s Hospital provides world class care and services to patients.
http://www.hmc.psu.edu/childrens/healthinfo/n/neurofibro.htm

71. DermAtlas: Online Dermatology Image Library Dermatology Image,neurofibromatosis,
DermAtlas Dermatology Images neurofibromatosis,neurofibroma,neurofibroma,dermatology image,café au lait spot, plexiform, plexiform images.
http://dermatlas.med.jhmi.edu/derm/result.cfm?Diagnosis=83

72. Neurofibromatosis
neurofibromatosis type I, or von Recklinghausen disease, is a autosomal dominant disorder affecting the neurofibromatosis type 1. Biochim Biophys Acta.
http://www.stevensorenson.com/residents6/neurofibromatosis.htm

Home
Up [ Neurofibromatosis ] Pyknodysostosis Mucopolysaccharidoses Multiple hereditary exostoses Ollier disease ... Dyschondrosteoses Neurofibromatosis type I, or von Recklinghausen disease, is a autosomal dominant disorder affecting the mesodermal and neuroectodermal tissues. Fifty percent of cases are due to spontaneous mutations. The incidence is 1 in 2,000 to 4,000 births. This is most common phakomatosis. Clinically, neurofibromas, cafe au lait spots, axillary/inguinal freckling, Lisch nodules (iris hamartomas), and osseous lesions are observed. A sharp angled scoliosis is characteristic of the disease, causing dwarfism. On occasion, the disease may produce a shortened limb due to bowing and pseudarthrosis, focal gigantism is more common, due to overgrowth of an ossification center, causing marked enlargement of a digit in the hand or foot. Treatment consists of scoliosis management. Usually, the scoliosis is refractory to bracing, and fusion may be required. REFERENCES Liebermann F, Korf BR. Emerging approaches toward the treatment of neurofibromatoses. Genet Med. 1999 May-Jun;1(4):158-64; quiz 165-6. Parada LF. Neurofibromatosis type 1. Biochim Biophys Acta. 2000 Jul 31;1471(1):M13-9.

73. ClinicalTrials.gov - Information On Clinical Trials And Human Research Studies:
Search results for neurofibromatosis ALLFIELDS are shown below. Conditions Neurofibroma, Plexiform; neurofibromatosis Type I
http://www.clinicaltrials.gov/search/term=Neurofibromatosis
Home Search Browse Resources ... About Search results for Neurofibromatosis [ALL-FIELDS] are shown below.
Include trials that are no longer recruiting patients.
9 studies were found. Recruiting R115777 to Treat Children with Neurofibromatosis Type 1 and Progressive Plexiform Neurofibromas
Conditions: Neurofibroma, Plexiform; Neurofibromatosis Type I Recruiting Pirfenidone in Children and Young Adults with Neurofibromatosis type I and Progressive Plexiform Neurofibromas
Conditions: Neurofibromatosis 1; Neurofibroma, Plexiform Recruiting An Implant for Hearing Loss Due to Removal of Neurofibromatosis 2 Tumors
Condition: Neurofibromatosis 2 Recruiting Fludeoxyglucose F 18 Positron Emission Tomography and Magnetic Resonance Perfusion Imaging in Patients With Neurofibromatosis 1 and Plexiform Neurofibroma
Condition: neurofibromatosis 1 and 2 (NF1 and NF2) Recruiting Study of Disease Severity in Adults with Neurofibromatosis Type 1 (NF1) Recruiting Tipifarnib in Preventing Cancer in Children With Neurofibromatosis Type 1 and Progressive Plexiform Neurofibromas
Conditions: childhood neurofibrosarcoma; childhood soft tissue sarcoma Recruiting Combination Chemotherapy in Treating Patients With Neurofibromatosis and Progressive Plexiform Neurofibromas
Conditions: childhood soft tissue sarcoma; childhood neurofibrosarcoma

74. Neurofibromatosis
with milk) colored blotches seen on the skin are the most recognized aspect of neurofibromatosis. Even so, these are not only seen in neurofibromatosis.
http://www.pediatric-orthopedics.com/Topics/Muscle_Neuro/Diseases/Neurofibromato
Neurofibromatosis The 'Cafe-au-Lait' (coffe with milk) colored blotches seen on the skin are the most recognized aspect of neurofibromatosis. Even so, these are not only seen in neurofibromatosis. Similar skin findings are found in Oliers's syndrome, Albright's disease, and Jaffe Campanacci syndrome - just to name a few. Also they are common in folks having no syndrome of any kind. At one time it was fashionable to use terms like phacodermatoses or neurocutaneous disorder. The gist was a wink wink implication of an embryological fact that is still hard to ignore. In the developing embryo , the nervous system starts out as a stripe down the center of the top embryologic layer. The embryo has an ectoderm (becomes skin and nervous system) separated from endoderm (guts, lips to tush) by mesoderm (meso means middle, it becomes muscle and bone). The whole thing rolls into a tube so that skin covers all. The central stripe of neuro-coulda-been-skin sinks in deep and is enveloped. Thus the nervous system is inside not outside. The edge - the very edge - where the neural ectoderm stripe touches plain old skin ectoderm - that edge is called the neural "crest". Why crest? Because as the skin and other stuff wells up to cover the neural stripe, this edge is on that crest. These neural crest cells are restless and do not stay put. They go on to migrate deep and go meandering into the other tissues to head the charge of neural tissue dispersing throughout other stuff.

75. Neurofibromatosis
neurofibromatosis is a rare inherited disorder that results in benign tumors of There are two types of neurofibromatosis. Type 1 (NF1), also called von
http://www.csmc.edu/5279.html

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Medical Dictionary Contact Us
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... Neurofibromatosis
Neurofibromatosis Neurofibromatosis is a rare inherited disorder that results in benign tumors of the nerves and other parts of the body. Symptoms of this disease range from being virtually unnoticeable to causing neurologic problems or bone defects that affect the skull and spine. Symptoms There are two types of neurofibromatosis. Type 1 (NF-1), also called von Recklinghausen's disease, causes multiple benign (noncancerous) tumors of the nerves and skin. Type 2 (NF-2) causes benign tumors of the nerves that transmit sound from the inner ears to the brain. In some cases, NF-2 causes visions problems and increases the risk of developing specific brain and spinal cord tumors. NF-1 can also cause a change in the color of the skin. Areas of unusual skin color may appear on the trunk of the body as well as cause freckling under the arms or in the groin area. Abnormal skin color may be seen in the patient by one year of age, and the area affected gets bigger over time. At birth or early childhood, patients may have rather large benign tumors that consist of bundles of nerves. They may also develop harmless tumor-like nodules of the colored parts of the eyes or tumors of the optic nerves, which send nerve impulses from the innermost membrane of the eyes (retinas) to the brain. More rarely, patients may develop certain malignant (cancerous) tumors.

76. Neurology - Neurofibromatosis
neurofibromatosis is a rare inherited disorder that results in benign tumors of the nerves There are two types of neurofibromatosis, Type 1 and Type 2.
http://www.csmc.edu/3007.html

Home
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... Trigeminal Neuralgia
Neurofibromatosis Neurofibromatosis is a rare inherited disorder that results in benign tumors of the nerves and other parts of the body. Symptoms of this disease range from being virtually unnoticeable to causing neurologic problems or bone defects that affect the skull and spine. There are two types of neurofibromatosis, Type 1 and Type 2.
Type 1 (NF-1), also called von Recklinghausen's disease, causes multiple benign (noncancerous) tumors of the nerves and skin. Type 2 (NF-2) causes benign tumors of the nerves that transmit sound from the inner ears to the brain. In some cases, NF-2 causes visions problems and increases the risk of developing specific brain and spinal cord tumors. NF-1 can also cause a change in the color of the skin. Areas of unusual skin color may appear on the trunk of the body, as well as freckling under the arms or in the groin area. Abnormal skin color may be seen in the patient by one year of age. Over time, the area affected gets bigger. At birth or early childhood, patients may have rather large benign tumors that consist of bundles of nerves. They may also develop harmless tumor-like nodules of the colored parts of the eyes or tumors of the optic nerves, which send nerve impulses from the innermost membrane of the eyes (retinas) to the brain. More rarely, patients may develop certain malignant (cancerous) tumors.

77. Neurofibromatosis

http://www.imgsrv.com/glossary/neurofibromatosis.html

78. Neurofibromatosis Definition - Medical Dictionary Definitions Of Popular Medical
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=4551

79. Acoustic Neurofibromatosis Definition - Medical Dictionary Definitions Of Popula
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=24463

80. Recklin1
neurofibromatosis. Von Recklinghausen neurofibromatosis. Patient with multiple neurofibromas. EXIT TO CONTENTS.
http://www.skinatlas.com/recklin1.htm
Neurofibromatosis Von Recklinghausen neurofibromatosis. Patient with multiple neurofibromas. EXIT TO CONTENTS

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