Extractions: This is a comprehensive atlas of the brain of the newborn infant as depicted by high-frequency ultrasound. For ease of use, the volume is arranged into distinct parts. Coverage begins with echo-anatomy, then proceeds through congenital anomalies, in utero acquired brain damage, and perinatal injury. Where relevant, corresponding CT or MRI pictures are provided. Additional topics covered include Doppler imaging and the measurement of echodensity. Throughout the work, the authors maintain a focus on relevance for the practicing physician. Thoroughly illustrated with over 600 halftones and color plates, this is an impressively up-to-date and comprehensive book.
Children's Hemiplegia And Stroke Association Children with Stroke, Cerebral Palsy, and porencephaly Sought for Study Investigatorsat the National Institute of Neurological Disorders and Stroke (NINDS http://www.chasa.org/researchninds.htm
Extractions: Investigators at the National Institute of Neurological Disorders and Stroke (NINDS) are seeking children with stroke, cerebral palsy, and porencephaly for a study of abnormal acquired and genetic coagulation factors. In the study, researchers will measure a series of potential risk factors for stroke that include autoimmune, inflammatory, and genetic clotting factor abnormalities. By identifying the factors that contribute to childhood stroke, cerebral palsy, and porencephaly, researchers hope this study will lay the groundwork for future research projects that will explore potential treatments. Eligible patients must have a history of porencephaly, cerebral infarction (stroke), and/or cerebral palsy and have a diagnosis of porencephaly or stroke confirmed by computed tomography (CT), magnetic resonance imaging (MRI), and/or Doppler ultrasonography. The study consists of a 30-minute telephone interview/questionnaire, blood sample, and buccal smear. All study-related expenses will be paid by the NIH. The study will be carried out under testing and safety standards of the U.S. Department of Health and Human Services.
Extractions: WebSearch Low-cost advertising at UKSprite Join Login @UK.Sprite Home Latest Headlines UK Weather World Weather ... UK Travel Guide Fun TV Guide Lotto e-Greetings Mobile Fun Communicate Email Login Get Free Email Free Text Messages Lifestyle Horoscopes Dating Recipes Health Shop DVD's Books Videos More... Deals Auctions Classified Ads Site Map
Untitled CASE IDENTIFICATION CODE UMB 1153 DISORDER porencephaly GESTATIONAL AGE 32 weeksSEX Male RACE Caucasian POST MORTEM INTERVAL 2 hour(s) KARYOTYPE AVAILABLE http://som1.umaryland.edu/BTBank/UMB_1153.htm
Extractions: AVAILABLE TISSUE ....FIXED.... BRAIN (Protocol Method 2) CEREBRUM- Hemi Coronal Section(2) OTHER ORGAN SYSTEMS GASTROINTESTINAL- (Liver), HEMATOPOIETIC- (Thymus), URINARY- (Kidney), OTHER TISSUE- (Tissue(s) nrc) ....FROZEN.... BRAIN (Protocol Method 2) CEREBRUM- Hemi Coronal Section(1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31), MID BRAIN/PONS- Section(1), CEREBELLUM- Section(1) OTHER ORGAN SYSTEMS CARDIOVASCULAR- (Heart), ENDOCRINE- (Thyroid), GASTROINTESTINAL- (Liver), GENITAL- (Testicle), HEMATOPOIETIC- (Thymus), MUSCULO SKELETAL- (Bone (rib), Diaphragm, Psoas), RESPIRATORY- (Lung), URINARY- (Kidney)
Medicalseek - Search Engine For The Healthcare Industry Conditions and DiseasesNeurological Disordersporencephaly MCW Health Link Anarticle about porencephaly, which is an extremely rare disorder of the central http://www.medicalseek.net/Conditions_and_Diseases_Neurological_Disorders_Porenc
Open Classes's $p->page_title Polska Svenska Open Directory Health Conditions and DiseasesNeurological Disorders porencephaly Previous Catagory. See http://dodo101.ath.cx/expat/odp.php/Health/Conditions_and_Diseases/Neurological_
Extractions: Open Directory Edit Add URL Update URL Description ... Svenska Open Directory - Health: Conditions and Diseases: Neurological Disorders: Porencephaly [ Previous Catagory See also: Open Directory - Health: Conditions and Diseases: Neurological Disorders: Porencephaly [ Previous Catagory All the Web AltaVista Deja Google ... Yahoo Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor
Suchmaschine Acoon - Webkatalog Top Health Conditions and Diseases Neurological Disorders porencephalyMCW Health Link An article about porencephaly, which http://www.acoon.de/cgi-bin/showcat.exe?cat=Top/Health/Conditions_and_Diseases/N
Extractions: N. Hayashi , Y. Tsutsumi and A. J. Barkovich Department of Radiology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan Section of Neuroradiology, University of California San Francisco, San Francisco, California, USA Department of Radiology, National Okura Hospital, Tokyo, Japan Abstract. Keywords. Polymicrogyria - MRI - Developmental anomaly E-mail: naoto-tky@umin.ac.jp
THE MERCK MANUAL, Sec. 19, Ch. 261, Congenital Anomalies Others (eg, hydranencephaly, porencephaly) occur later and appear tobe secondary to destructive processes after the brain has formed. http://www.merck.com/pubs/mmanual/section19/chapter261/261h.htm
Extractions: This Publication Is Searchable The Merck Manual of Diagnosis and Therapy Section 19. Pediatrics Chapter 261. Congenital Anomalies Topics [General] Congenital Heart Disease Pulmonary Vascular Disease Heart Failure ... Chromosomal Abnormalities Neurologic Abnormalities Some of the most serious neurologic abnormalities (eg, anencephaly, encephalocele, spina bifida) develop in the first 2 mo of gestation and represent defects in neural tube formation (dysraphia). Others (eg, hydranencephaly, porencephaly) occur later and appear to be secondary to destructive processes after the brain has formed. Some defects are relatively benign (eg, meningocele). Accurate in utero detection of many malformations is now possible using amniocentesis and ultrasonography (see also Ch. 247 ). Genetic counseling for parents of a child with a major neurologic abnormality is important, since the risk of a subsequent child's having such a defect is high. These parents also need psychologic help and support. Women who have had a pregnancy resulting in an infant or fetus with a neural tube defect should be advised that folic acid supplementation (4 mg/day) before conception and during early pregnancy may substantially reduce the risk of neural tube defects in subsequent pregnancies. BRAIN ABNORMALITIES Anencephaly
Fetal MR Imaging At BIDMC (D. Levine, M.D.) 642. porencephaly Destruction of brain tissue Moderate ventriculomegalywith porencephaly in a 38 week gestational age fetus. http://www.bidmc.harvard.edu/radiology/research/ultrasound/us_fetalmr/fetalMR.ht
Extractions: Magnetic resonance (MR) imaging is a valuable complement to ultrasound when additional information is needed to make treatment decisions during pregnancy. In the past studies were limited by fetal motion. Due to fast imaging techniques now available, images can be obtained in less than 1/2 a second. This means that neither the mother nor the fetus needs to be sedated. One area where MR imaging has proven to be especially beneficial is in evaluation of the fetal CNS . Multiplanar views can be difficult to obtain with sonography due to fetal position or advanced gestational age. MR imaging can be used to obtain multiplanar views. In addition, MR imaging allows for direct visualization of the brain parenchyma and thus allows for detailed evaluation of the CNS anatomy in a manner not possible with sonography. There is no known risk to fetal MRI, but due to theoretic concerns, we avoid scanning in the first trimester. In an ongoing study, we have evaluated fetal CNS abnormalities with ultrasound and MR imaging. To date, over 115 fetuses have undergone MR examinations for sonographically suspected CNS abnormalities. In all cases MR imaging demonstrated the region of US abnormality. In over half of cases, the information provided by MR imaging was of the type which warranted changes in patient counseling or management. Encephalocele Sagittal view of a posterior encephalocele in a 32 week gestational age fetus. Only a small portion of posterior cortex is tented toward the defect. At surgery, the encephalocele was removed and a small portion of cortex was pushed back into the cranial vault without difficulty. Reproduced with permission from AJR 1999;172:813-818.
Targeted Ultrasound (LEVEL II) BACK TO TOP OF PAGE porencephaly. Localized atrophy causing cystic cavitiesin cerebral matter from primary maldevelopment (schizencephaly http://192.215.104.222/obgyn/PUBLIC/ULTRASOU/US4.htm
Targeted Ultrasound (LEVEL II) Search Literature. BACK TO TOP OF PAGE porencephaly. Localized atrophycausing cystic cavities in cerebral matter from primary maldevelopment http://192.215.104.222/obgyn/PUBLIC/ULTRASOU/us4.htm
Untitled B. Holoprosencephaly. C. Lissencephaly. D. porencephaly. E. Arhinencephaly. A. Encephalocele.B. Meningomyelocele. C. porencephaly. D. Internal hydrocephalus. http://www.indstate.edu/thcme/anderson/mcdevel.html
Extractions: DEVELOPMENT TEST MULTIPLE CHOICE QUESTIONS 1. All of the following could result in alteration of cell mitosis postnatal brain development except A. Hyperthyroidism. B. Neurofibrillary degeneration. C. Malnutrition. D. Radiation damage. E. Environmental complexity. 2. Which of the following is incorrect in regard to the five vesicle stage of the embryonic brain: A. Prosencephalon. B. Diencephalon. C. Mesencephalon. D. Myelencephalon. E. Metencephalon. 3. Embryonic neurohistogenesis is characterized by: A. A continual proliferation of neuroblasts without any sequencing. B. Neurons differentiating at the site of proliferation. C. Mitosis occurring at the outermost portion of the neuroepithelium. D. Production of small neurons before large neurons. E. Production of a new proliferative matrix in the cerebellum and cerebral cortex. 4. Spongioblasts refer to: A. Misplaced neurons. B. Another name for neural crest cells. C. Neuroglia. D. Newly formed blood vessels. E. Choroid plexus cells. 5. All of the following are
Porencephaly In Health > Conditions And Diseases > Neurological Disorders Similar pages www.wholesaledropshipping.com/catalog.php/Health/Conditions_and_Diseases/Neurological_Disorders/porencephaly/ Similar pages THE LIGHTNING HYPERTEXT OF DISEASE. key words inherited, pediatric, JB Packet No. 4 25210 porencephaly familial=hemiplegia infantile with porencephaly key words terminology, JB http://ilectric.com/browse/web/Health/Conditions_and_Diseases/Neurological_Disor
Extractions: Metasearch Directory News Multi-Search ... Login/Out Choose a Search Metasearch - The Web Metasearch - This Site Metasearch - News Metasearch - Auctions Metasearch - Forums Metasearch - Images Metasearch - Shopping Directory - Within This Category Only Directory - Entire Directory - Adult Directory - Arts Directory - Business Directory - Computers Directory - Games Directory - Health Directory - Home Directory - News Directory - Recreation Directory - Reference Directory - Regional Directory - Science Directory - Shopping Directory - Society Directory - Sports Directory - World Shopping - All products Shopping - Books Shopping - Electronics Shopping - Popular music Shopping - Classical music Shopping - DVD's Shopping - VHS Videos Shopping - In Theaters Shopping - Toys Shopping - Computer Hardware Shopping - Software Shopping - Magazines Shopping - Photo Shopping - Garden / Outdoor Living Shopping - Baby Shopping - Kitchen Lookup - Domain in Whois Lookup - Domain Availability Lookup - HTTP Source Lookup - DNS Record Categories Related Sponsored Sites Sites ... Neurological Disorders Porencephaly
2105 Challenges In The Prenatal Diagnosis Of Walker-Warburg Fetal head MRI showed severe hydrocephalus,porencephaly,a nondilated 4th ventricle,and cerebellar hypoplasia. The corpus callosum was not visualized. http://www.faseb.org/genetics/ashg99/f2105.htm
SearchUK Home Top Health Conditions_and_Diseases Neurological_Disorders porencephaly. ADULT (18+), SHOPPING, FINANCE, GAMBLING, JOBS, TRAVEL, http://www.searchuk.co.uk/Top/Health/Conditions_and_Diseases/Neurological_Disord
Callosal Agenesis 2001 Record 6 of 12 in MEDLINE(R) on CD 2001. TITLE Familial orofaciodigital syndrometype I revealed by ultrasound prenatal diagnosis of porencephaly. http://www.indiana.edu/~pietsch/acc2001.html
Extractions: go to Shufflebrain main menu return to ACC Menu web contact: pietsch@indiana.edu A search of Medline at Indiana University, Bloomington, Indiana The following items were compiled by SilverPlatter and are presented with their permission. ( See SilverPlatter's Worldwide Library for bibliographic search information < Record 1 of 12 in MEDLINE(R) on CD 2002/01 TITLE: Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene. AUTHOR: Weller,-S; Gartner,-J ADDRESS OF AUTHOR: Department of Pediatrics, Heinrich Heine University, Dusseldorf, Germany. SOURCE: Hum-Mutat. 2001; 18(1): 1-12 INTERNATIONAL STANDARD SERIAL NUMBER: 1098-1004 PUBLICATION YEAR: 2001 LANGUAGE: English COUNTRY OF PUBLICATION: United-States MAJOR MESH DESCRIPTORS: *Abnormalities,-Multiple-genetics; *Hydrocephalus-genetics; *Linkage-Genetics-genetics; *Membrane-Glycoproteins-genetics; *Mutation-genetics; *Neural-Cell-Adhesion-Molecules-genetics; *X-Chromosome-genetics MINOR MESH DESCRIPTORS: Abnormalities,-Multiple-diagnosis; Abnormalities,-Multiple-physiopathology; Genotype-; Hydrocephalus-diagnosis; Hydrocephalus-physiopathology; Introns-genetics; Membrane-Glycoproteins-chemistry; Molecular-Sequence-Data; Neural-Cell-Adhesion-Molecules-chemistry; Phenotype-; Polymorphism-Genetics-genetics; RNA-Splice-Sites-genetics; Syndrome-
Sod-medline.html is welldocumented for gastroschisis, but similar findings with hydranencephalysuggest a general phenomenon that may also involve porencephaly, septo-optic http://www.indiana.edu/~pietsch/sod-medline.html
Extractions: The following MEDLINE items were compiled by SilverPlatter and are presented with their generous co-operation and permission. ( See SilverPlatter's Worldwide Library for bibliographic search information Record 1 of 30 in MEDLINE EXPRESS (R) 1996-1998 TITLE: Normal growth in a patient with septo-optic dysplasia despite both growth hormone and IGF-I deficiency. AUTHOR(S): Bereket-A; Lang-CH; Geffner-ME; Wilson-TA ADDRESS OF AUTHOR: Department of Pediatrics, Hacettepe University, Ankara, Turkey. SOURCE (BIBLIOGRAPHIC CITATION): J-Pediatr-Endocrinol-Metab. 1998 Jan-Feb; 11(1): 69-75 LANGUAGE OF ARTICLE: ENGLISH COUNTRY OF PUBLICATION: ENGLAND MEDLINE ACCESSION NUMBER: 1998306600 Record 2 of 30 in MEDLINE EXPRESS (R) 1996-1998 TITLE: [Septo-optic dysplasia (de Morsier syndrome)] AUTHOR(S): Stangel-M; Vogeley-KT; Jandeck-C; Boegner-F; Marx-P; Koch-HC ADDRESS OF AUTHOR: Abteilung fur Neurologie, Universitatsklinikum Benjamin Franklin, Freie Universitat Berlin.
