61. EMedicine - Hyperhidrosis : Article By Robert A Schwartz, MD, MPH Chronic alcoholism Hodgkin disease Tuberculosis Eccrine nevus Eccrine angiomatoushamartoma rileyday syndrome (familial dysautonomia) http://www.emedicine.com/derm/topic893.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Dermatology Diseases Of The Adnexa Hyperhidrosis Last Updated: August 23, 2005 Rate this Article Email to a Colleague Synonyms and related keywords: excessive sweating, palmoplantar hyperhidrosis, emotionally induced hyperhidrosis, generalized hyperhidrosis, localized hyperhidrosis, palmoplantar sweating, axillary hyperhidrosis, nocturnal hyperhidrosis AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Robert A Schwartz, MD, MPH , Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School Coauthor(s): Rachel Altman, MD , Consulting Staff, Department of Dermatology, Rush University Medical Center; Robert A Schwartz, MD, MPH , Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School George Kihiczak, MD

62. Disease, Medication, Symptom Etc Database Index : R Diseases Database rileyday syndrome see Hereditary sensory and autonomic neuropathy type 3 Riley-Smith syndrome Rilmenidine Riluzole Rimantadine Rimexolone http://www.diseasesdatabase.com/disease_index_r.asp

Diseases Database Index Sponsors Contact ... Previous Page Disease, medication, symptom etc database index : R Search RA see Rheumatoid disease Rabeprazole Rabies Rabson-Mendenhall syndrome Raccoon roundworm see Baylisascariasis Racecadotril see Acetorphan Radial agenesis see Radial hypoplasia Radial aplasia-thrombocytopenia syndrome Radial hypoplasia Radiation sensitizing drugs see Radiosensitizing agents Radiculitis Radiculopathy Radiology result abnormal see X-ray abnormality Radiosensitizing agents Radiotherapy Raeder paratrigeminal syndrome Raeder-Harbitz syndrome see Takayasu's arteritis Raised intracranial pressure Raised intraocular pressure Ralitrexed see Raltitrexed Raloxifene RALPH syndrome see Pallister-Hall syndrome Ralstonia Raltitrexed Ramelteon ... Ramosetron Ramsay Hunt cerebellar syndrome see Cerebellar dyssynergia Ramsay Hunt syndrome Ranibizumab Ranitidine ... Rapacuronium Rapamycin see Sirolimus Rapid up-stroke pulse Rapp-Hodgkin ectodermal dysplasia syndrome Rasagiline ... Rasmussen encephalitis Rat tapeworm infection see Hymenolepiasis Rathbun syndrome see Phosphoethanolaminuria Rathke cleft cysts Rathke's pouch tumor see Craniopharyngioma Rauwolfia alkaloids Ravuconazole Raymond Cestan syndrome Raymond-Foville syndrome see Millard-Gubler syndrome Raynaud's disease Raynaud's phenomenon Razoxane RBBB see Right bundle branch block Reactive arthropathy Reactive lymphocyte see Atypical lymphocytes Reactive lymphoid hyperplasia see Pseudolymphoma Reactive perforating collagenosis REAR syndrome see Townes-Brocks syndrome Reaven syndrome X Reboxetine Recessive deafness-onychodystrophy-osteodystrophy-retardation syndrome Recrudescent typhus

63. Mitral Valve Prolapse There is a genetic form of dysautonomia, called rileyday syndrome, most frequently,if not exclusively, found in families of European Jewish descent. http://www.icorp.net/cardio/articles/mvp-dys.htm

64. FIRSTConsult - Sdfdsf rileyday syndrome, congenital insensitivity to pain, and a number of hereditary riley-day syndrome, Charcot-Marie-Tooth, other inherited neuropathies, http://www.firstconsult.com/?action=view_article&id=1014518&type=101&bref=1

65. CONGENITAL INSENSITIVITY/INDIFFERENCE TO PAIN: Contact A Family - For Families It is also known as the rileyday syndrome or Familial Dysautonomia. While FDoccurs almost exclusively in Ashkenazi Jews, riley-day syndrome occurs in the http://www.cafamily.org.uk/Direct/c645.html

printer friendly CONGENITAL INSENSITIVITY/INDIFFERENCE TO PAIN home how we can help medical information index of conditions ... how you can help Did you find this page helpful? yes no Congenital Insensitivity to Pain: Congenital Indifference to Pain; Hereditary and Sensory Autonomic Neuropathy Types I-IV; HSAN Types I-IV In Congenital Insensitivity to Pain, there are structural abnormalities in peripheral nerves which are the peripheral pathways carrying electrical impulses from pain sensitive nerve endings in both superficial and deep tissues. In Congenital Indifference to Pain, the peripheral nerves are intact and the defect is apparently in the central structures such as the thalamus where painful impulses are normally interpreted. However, it is now thought that some individuals, formerly given a diagnosis of Congenital Indifference to Pain, have been shown by refined histological techniques, which look at the minute structures of bodies, to also have peripheral nerve abnormalities and are therefore examples of Congenital Insensitivity to Pain. Nevertheless, Congenital Indifference to Pain almost certainly exists as an independent condition, but is very rare. Congenital Insensitivity to Pain (of which types I to IV are generally accepted, with some other very rare conditions) is usually classified under the more general heading of Hereditary and Sensory Autonomic Neuropathy (HSAN). The various categories are distinguished according to clinical features, including age of onset, progressive or non-progressive, presence or absence of abnormalities of the autonomic nervous system, if the system is sympathetic (augmenting actions) or parasympathetic (inhibiting actions) and also according to the nature of structural abnormalities in peripheral nerves.

66. Index R: Contact A Family - For Families With Disabled Children: Information On Right Atrial Isomerism see Ivemark syndrome rileyday syndrome see Metabolicdiseases Robin Anomalad see Pierre Robin syndrome http://www.cafamily.org.uk/Idx/r.html

printer friendly home how we can help medical information ... how you can help Please use the index below to access the condition you require information on. It may take longer to find what you are looking for this way compared with our "search this site" facility in the navigator on the left but we try to point you in the most appropriate direction using this index and therefore the results should be better. For speed, this index has been split into separate alphabetical files: numbers 0-9 A B C ... Z Contact a Family also has information on many other specific conditions and rare disorders. If you cannot find the information you require in The Contact a Family Directory Online , you may wish to use our Contact a Family Helpline service. RE see Rasmussen's Encephalitis RSMD1 see Congenital Muscular Dystrophy RSV see Lung diseases Rasmussen's Encephalitis Rasmussen's syndrome see Rasmussen's Encephalitis Raynaud's Phenomenon Reading Disorders see Dyslexia Recessive Spino-cerebellar Degeneration see Friedreich's Ataxia Reflex Anoxic Seizures Reflex Sympathetic Dystrophy Refsum's disease see Ichthyosis Reifenstein syndrome see Androgen Insensitivity syndrome Relapsing Polychondritis Renal Failure see Kidney disease Rendu-Osler-Weber see Hereditary Haemorrhagic Telangiectasia Respiratory Chain Disorders see Mitochondrial Cytopathies and related disorders Respiratory Syncytial Virus see Lung diseases Restricted Growth Reticular Dysgenesis see

67. APA Books Familial Dysautonomia (rileyday syndrome) Paul J. Meller, Paula Larson, andCheryl Engel. 40. Fetal Alcohol Syndrome Jacqueline J. Smith and Janet L. http://www.apa.org/books/4312060t.html

APA Members/ Affiliates: List: $39.95 Item # 4312060 ISBN: Health-Related Disorders in Children and Adolescents : A Guidebook for Understanding and Educating: Contents "Editor: LeAdelle Phelps" May 1998 Hardcover 743 Pages Table of Contents List of Contributors Acknowledgments Part I: Background Information 1. How to Use This Book LeAdelle Phelps 2. A Guide to Genetics LeAdelle Phelps 3. Role of the School-Based Professional in Health-Related Services Thomas J. Power, George J. DuPaul, Edward S. Shapiro, and John M. Parrish Part II: Health-Related Disorders 4. Achondroplasia (Dwarfism) Georgia Frey and Douglas Palmer 5. Adrenoleukodystrophy Harvey N. Switzky, James P. Van Haneghan, and Abigail Baxter 6. Albinism Frank Murtha 7. Angelman Syndrome Richard J. Morris and Yuonne P. Morris 8. Apert Syndrome (Acrocephalosyndactyly Type I) Georgia Frey and Douglas Palmer 9. Arthritis (Juvenile Rheumatoid) Eric L. Robinson 10. Asperger's Disorder

68. Cyclic Vomiting Syndrome (CVS) - Pathopysiology One extreme example, rileyday syndrome (familial dysautonomia), manifests asboth autonomic dysfunction and episodic vomiting (Axelrod, 1991). http://www.cvsaonline.org/diseaseresearchinfomedicalinfopathophysiology.htm

Pathophysiology The pathophysiology of CVS is elusive. Recently, several potential brain-gut mechanisms have been postulated. Support exists for migraine-related mechanisms, and neuronal hyperexcitability is a potential cause of CVS. Because most patients have a family history of migraine (82% vs 14% of control subjects with a chronic vomiting pattern), the authors suspect that these central mechanisms cause both migraines and CVS. In specific migraine subtypes, neuronal hyperexcitability can be induced by reduced mitochondrial energy production and altered intracellular divalent cation concentrations. For example, patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome experience both CVS and classic migraines related to defective peripheral and central cellular respiratory chain metabolism. Additionally, familial hemiplegic migraines are caused by cortical hyperexcitability due to altered permeability of voltage-gated calcium channels (Cullen, 1963). Other mitochondrial DNA mutations may be involved in the pathogenesis of CVS. Researchers know that 80% of children with CVS have familial migraines on the maternal side only. Boles and colleagues reported a large mitochondrial DNA deletion in a single child with CVS, and they have identified additional mutations concentrated in the D-loop (control region) in other children with CVS (Boles, 1997; Boles, 1999).

69. CMT Mutations Familial dysautonomia or rileyday syndrome or HSN III. htz/hmz. compound htz.Family History. AR. Deduced RE sites. +HphI / -. Anderson et al., 2001 http://www.molgen.ua.ac.be/CMTMutations/DataSource/Mutations.cfm?Context=14

70. Essence Of Anaesthesia Practice Familial Dysautonomia (rileyday syndrome) Familial Periodic Paralysis (Hyperkalemic)Familial Periodic Paralysis (Hypokalemic) Fat Embolism http://www.mitec.com.au/catalogue/category392/category771/product10825

Mi-tec Medical Publishing Home SEARCH Staff About Us ... Contact Us ASA Bookshop General Essence of Anaesthesia Practice Here's remarkably convenient access to essential anesthesia considerations for a full range of common and uncommon diseases. Every page covers a single clinical topic-over 600 in all-presenting important information in an extremely accessible fashion. Divided into 5 sections - * Diseases * Procedures * Drugs * Alternative Medicine * and Tests, with topics within each section organized alphabetically-this resource allows readers to approach a given problem from any of these directions to find the answers they need. The 2nd Edition has been thoroughly revised and updated to encompass the latest developments in the field. Features: * Offers a one-of-a-kind format in which relevant information can be found in the same place on each page. * Features an international team of expert contributing authors-ensuring information is state-of-the-art and reliable. * Describes common drugs and alternative medicine drugs taken by patients that must be considered before anesthetizing. * Includes detailed coverage on both the common and rare conditions patients present with and how the anesthesiologist must consider each.

71. Elsevier.com - Systemic Diseases And The Eye Rieger syndrome rileyday syndrome (familial dysautonomia) Rosacea SarcoidosisSchilder disease Sjogren syndrome Stevens-Johnson syndrome (erythema http://www.elsevier.com/wps/product/cws_home/698014

Home Site map Regional Sites Advanced Product Search ... Systemic Diseases and the Eye Book information Product description Audience Author information and services Ordering information Bibliographic and ordering information Book related information Submit your book proposal Other books in same subject area About Elsevier Select your view SYSTEMIC DISEASES AND THE EYE Clinical Signs and Differential Diagnosis To order this title, and for more information, go to http://www.elsevierhealth.com/title.cfm?ISBN=0723432163 First Edition By Jack Kanski , MD, MS, FRCS, FRCOphth, Honorary Consultant Ophthalmic Surgeon, Prince Charles Eye Unit, King Edward VII Hospital, Windsor, UK Description SYSTEMIC DISEASES AND THE EYE leads ophthalmologists away from looking only at the eye and toward viewing the patient as a whole. This approach aids the ophthalmologist in making an accurate differential diagnosis. The text comprehensively covers all systemic diseases associated with the eye. The book is divided into three parts, each approaching ocular conditions from a different viewpoint. Part One is lavishly illustrated in full color. It describes different ocular conditions and related signs and gives the systemic diseases associated with them. Part Two is also filled with illustrations and covers the differential diagnosis of systemic signs. Part Three links the different ocular and systemic features and signs together. The illustrations are enhanced throughout with brief, bullet-point text that follows a consistent format for ease of reference.

72. Elsevier.com - Essence Of Anesthesia Practice MetabolicEncephalopathy, Postanoxic Endocardial Cushion DefectEpidermolysisBullosaEpiglottitisFamilial Dysautonomia (rileyday syndrome)Familial http://www.elsevier.com/wps/product/cws_home/691710

Home Site map Regional Sites Advanced Product Search ... Essence of Anesthesia Practice Book information Product description Audience Author information and services Ordering information Bibliographic and ordering information Book related information Submit your book proposal Other books in same subject area About Elsevier Select your view ESSENCE OF ANESTHESIA PRACTICE To order this title, and for more information, go to http://www.elsevierhealth.com/title.cfm?ISBN=0721692672 Second Edition By Michael Roizen , MD, Dean of the School of Medicine and Vice President of Biomedical Affairs, Professor of Internal Medicine and Anesthesiology, SUNY Upstate Medical University, Syracuse, NY Lee Fleisher , MD, Dripps Professor and Chairman, Department of Anesthesia; Professor, Department of Internal Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania Description Here's remarkably convenient access to essential anesthesia considerations for a full range of common and uncommon diseases. Every page covers a single clinical topic*nearly 600 in all*presenting important information in an extremely accessible fashion. Divided into five sections*Diseases, Procedures, Drugs, Alternative Medicine, and Tests, with topics within each section organized alphabetically*this resource allows readers to approach a given problem from any of these directions to find the answers they need. The second edition has been thoroughly revised and updated to encompass the latest developments in the field. Audience

73. 223900 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 HSAN III DYSAUTONOMIA, FAMILIAL; DYS; FD rileyday syndrome Goldstein-Nieviazhski,C.; Wallis, K. riley-day syndrome (familial dysautonomia) survey http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:223900] -e

74. MUMS List Of Disorders - F - G FG Syndrome (17) *FG Syndrome Home Page; Fabry Disease (3) Polyposis (GardnerSyndrome) (3); Familial Dysautonomia (rileyday syndrome) (8)** http://www.netnet.net/mums/mum_f-g.htm

Return to MUMS Home Page MUMS: List of Disorders F - G Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. FG Syndrome (17) * FG Syndrome Home Page Fabry Disease (3) * Facial Cleft (4) Facio-Auriculo-Vertebral Spectrum (Goldenhar Syndrome) (82) ** Facio-Scapulo-Humeral Dystrophy, Infantile (FSH) (3) * Facioscapuloperoneal Dystrophy, Infantile (1) Factor IV Deficiency (1) Factor V Deficiency (2) Factor XI Deficiency (1) Factor XIII Deficiency (1) Fahr's Disease (1) Failure To Thrive (212) Fainting Spells, Undiagnosed (3) Familial Adenomatous Polyposis (Gardner Syndrome) (3) Familial Dysautonomia (Riley-Day Syndrome) (8)** www.fdvillage.org/ Familial Erythrophagocytic Lymphohistiocytosis (1) * Familial Exuderitive Vitrio (1) Familial Mediteranean Fever (3) Familial Spastic Diplegia (Paraparesis or Paraplegia) (7) Fecal Retention Syndrome (following imperforate anus surgery) (3) Feet not growing (1) Feingold Syndrome (Oculo-Digit-Esophageal-Duodenum (ODED) (1) Femoral Antiversion (1) Femoral Focal Deficiency, Proximal (PFFD) (10)*

75. MUMS List Of Disorders - Q - R Rieger Anomaly (eye, anterior segment dysgenesis) (8) *; Rieger Anomalygrowthretardation (SHORT Syndrome) (1); riley-day syndrome (Dysautonomia, http://www.netnet.net/mums/mum_q-r.htm

Return to MUMS Home Page MUMS: List of Disorders Q - R Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. Quadriplegia (213) Quadruplets 2 w/Cerebral Palsy (1) Quadruplets 2 w/Cerebral Palsy/2 died (1) Radial Club Hand (5) * Radio-Sensitivity (1) Radio-Ulnar Synostosis, Bilateral (arms can't rotate) (1) Radio-Ulnar Synostosis, Unilateral (right arm can't rotate) (1) Rasmussen Syndrome (4) * Rathke's Pouch Tumor (1) Raynaud's Disease and Phenomenon (5) * Reactive Airway Disease (34) Rectal Malformation (69) * Redman Syndrome from Vancomycin (1) Reflex Anoxic Seizures (2) * Reflex Sympathetic Dystrophy Syndrome (8) ** Refsum Syndrome (5) Refsum Syndrome, Infantile (2) Reiter Syndrome (Ankylosing Spondylitis) (1) Renal Acidosis (1) Renal Agenesis, Bilateral (2) Renal Agenesis, Unilateral (2) Renal Dysplasia (2) Renal Failure, Chronic (19) * Renal Tubular Acidosis (13) * Renal, Fanconi Syndrome (4) * Respiratory Distress Syndrome (RDS) (33) Respiratory Syncitial Virus (RSD) (39) Restrictive Cardiomyopathy Ideopathic Heart Disease (1) * Restrictive Lung Disease (4) Retinal Angiomata (1) Retinitis Pigmentosa (RP) (17) * Retinoblastoma (11) * Retinopathy of Prematurity (58) * Retinoschisis, Juvenile (2)

76. SEMERC: Information Services: Glossary: R rileyday syndrome or Familial Dysautonomia Types 1 2. Features includeswallowing difficulty, vomiting, breath-holding attacks in infancy, blotchy skin, http://www.semerc.com/information_services/a_z/r.asp

Search our online shop SEMERC Information Services: Glossary : Q The SEMERC Glossary is kindly provided by David Fulton Publishing. Click on a letter to jump to the appropriate page. A B C D ... Z Rate Recording A term used in behaviour modification to denote the recording of the number of times a behaviour has occurred Receptive Aphasia Impairment of the understanding of language. Recessive Gene A gene which is the weaker of a pair and whose characteristic is only expressed if paired with another recessive gene for the same characteristic. (See also Autosomal Recessive Disorder) Reflex Arc The system of sensory and motor neurones which carry out a reflex action. Reinforcement, Negative A term used in behaviour modification to denote the withdrawal of something a person dislikes, or of a punishment, so that the individual learns that he can remove it by appropriate behaviour. Reinforcement, Positive A term used in behaviour modification to denote the provision of something a person likes, or a reward, to encourage appropriate behaviour.

77. Familial Dysautonomia And The Brain Behavior Enigma Familial Dysautonomia (FD), also called rileyday syndrome, is one of fivehereditary sensory and autonomic neuropathies (HSANS) (2). http://serendip.brynmawr.edu/bb/neuro/neuro01/web1/Brennan.html

This paper reflects the research and thoughts of a student at the time the paper was written for a course at Bryn Mawr College. Like other materials on Serendip , it is not intended to be "authoritative" but rather to help others further develop their own explorations. Web links were active as of the time the paper was posted but are not updated Contribute Thoughts Search Serendip for Other Papers Serendip Home Page Biology 202 ... 2000 First Web Report On Serendip Familial Dysautonomia and the Brain Behavior Enigma Avis Brennan An understanding of the brain is essential to developing safe and effective treatments for disorders of the nervous system and for advancing our understanding of the human experience. Nervous system disorders cost the US more than $400 billion in medical expenses each year . In addition to having great clinical significance, such research offers a valuable perspective into the nature of the brain-behavior relationship. The extent to which the brain is organized in terms of overt behavior remains an open question. Because it is difficult to ethically manipulate the neural composition of humans in the laboratory setting, our understanding of the biological and neurophysiological influences on behavior is limited. In the spirit of this class, I have decided to take an alternate route to untangling the connections between brain and behavior. In this paper, I will discuss Familial Dysautonomia, a neurological disease that encapsulates the relationship between sensation, perception, emotion, physiological response and the nervous system.

78. J. - Toddler Dies In S.F. After Battling Rare Genetic Disease Familial dysautonomia, or rileyday syndrome, is so rare that only 480 cases She remembered that as being a symptom of riley-day syndrome and sent the http://www.jewishsf.com/content/2-0-/module/displaystory/story_id/7608/edition_i

Friday December 12, 1997 - Thursday December 18, 1997 Printer Friendly Email to A Friend Friday December 12, 1997 Toddler dies in S.F. after battling rare genetic disease LESLIE KATZ Bulletin Staff A San Francisco toddler with a rare genetic disorder that afflicts only Ashkenazic Jews died this week at nearly 3-1/2 years old. Isa Leah Cymrot-Wu died after an ear infection led to a string of complications related to her disease, familial dysautonomia. "She's like a comet that flew through the sky and our lives," said her mother, Dafna Wu, who co-parented the child with partner Barbara Cymrot. "She just shone so brightly. She beamed." In March of last year, the Bulletin ran a story about the young girl's odyssey. Jewish Family and Children's Services had started a fund to help her parents defray the significant medical costs involved with their child's treatment, which required trips to New York to see an expert on the disease. Familial dysautonomia, or Riley-Day Syndrome, is so rare that only 480 cases worldwide have been reported since 1970. Other than one reported case in San Jose, young Cymrot-Wu was believed to be the only Bay Area baby with the illness. Born on July 20, 1994, Cymrot-Wu exhibited a bizarre array of symptoms almost from the start. Fevers rose and fell without obvious cause. Her limbs appeared floppy. She would gulp and swallow air. She couldn't produce tears. For the first 10 months of her life, she underwent a battery of tests to try and pinpoint the symptoms; all proved inconclusive.

79. CFS By Other Names 1965 Familial Dysautonomia, AKA rileyday syndrome 1965 Asthenic Neurosis 1966Psycho-Vegetative Syndrome 1968 Pseudoneurasthenic Syndrome http://www.cssa-inc.org/Articles/CFS_names.htm

Home Newsletter Pamphlet News and Events ... Links CFS by other names... In my play on The Illness and Death of Edgar Allan Poe (presented Monday to a standing room only crowd at the National Library of Medicine that really liked it), I included the following list of all the many names that I have found for the syndrome first named neurasthenia in April 1869, up to the most recent proposal of Chronic Neuroendocrineimmune Dysfunction Syndrome. (I'm sure there are still some I've missed! Please let me know if you know of more). The dates refer to the year of the earliest (and often only one) published paper I could find that defines the disease. I posted an earlier version of this some years ago. This one is considerably expanded and may be reposted freely provided this text is kept with it and the list is not changed in any way. Albert Donnay, MCSRR Neurasthenia and its subtypes 1869 Neurasthenia 1869 Neurasthenia (undifferentiated) 1889 Neurasthenia Praecox 1891 Female Neurasthenia 1893 Syphilitic Neurasthenia 1895 Senile Neurasthenia 1875 Spinal Neurasthenia, AKA Railway Spine

80. Sleep Disturbance In Children And Adolescents With Disorders Of Development - Ca Sleep disorders and PraderWilli syndrome Antonio Vela Bueno, Olivan-Palacios achondroplasia; Leigh’s syndrome; riley-day syndrome; Moebius syndrome; http://www.cambridge.org/uk/catalogue/catalogue.asp?isbn=1898683247

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