81. Entrez-PubMed read Fine mapping of the locus for shwachmanDiamond syndrome at 7q11, identificationof shared disease haplotypes, and exclusion of TPST1 as a candidate gene. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

82. Shwachman-Diamond Syndrome Canada Translate this page Alérion shwachman-Diamond syndrome Canada. PO Box 502 WolfvilleNova Scotia B0P 1X0 Projets actifs à l'Université Laval. http://www.ulaval.ca/vrr/rech/Prog/org010356.html

Shwachman-Diamond Syndrome Canada P.O. Box 502 Wolfville Nova Scotia Programmes de recherche Subvention de recherche

83. Shwachman-Diamond Syndrome Canada Translate this page Alérion shwachman-Diamond syndrome Canada. PO Box 502 Wolfville Nova ScotiaB0P 1X0 Programmes de recherche. Projets actifs à l'Université Laval http://www.ulaval.ca/vrr/rech/Proj/org010356.html

Shwachman-Diamond Syndrome Canada P.O. Box 502 Wolfville Nova Scotia Programmes de recherche

84. Shwachman Diamond Syndrome shwachman Diamond syndrome. shwachman Diamond syndrome is a rare condition that involvesthe pancreas and bone marrow it makes them unable to function normally. http://members.tripod.com/shwachmandiamondkids/

Get Five DVDs for $.49 each. Join now. Tell me when this page is updated Welcome to Shwachman Diamond Kids the Home of Brandons Dream Team We Thank You for stopping by to visit! Brandon loves his TIVO! Our prayers go out to Jeff, Dani's Fiancé'. He is in the desert now! We are thinking of you Jeff. God Bless the USA!!! Shwachman Diamond Syndrome Shwachman Diamond Syndrome is a rare condition that involves the pancreas and bone marrow it makes them unable to function normally. It is usually diagnosed in infancy or early childhood and is an inherited condition. This condition causes the pancreas to not function properly, therefore they are unable to digest food properly. This leads to the difficulty gaining weight. The Bone Marrow may not produce all of the blood cells in normal number, especially infection fighting white blood cells. These are called Neutrophils. Bone Marrow failure may develop over time. Other things associated with SDS are short stature, skeletal abnormalities, learning difficulties, frequent infections, liver, kidney and dental problems. It is important to know that not all children born with SDS will have all of the symptoms of the disease. Brandon does not have all of the signs and symptoms of SDS. He has many of them. His lifestyle is much different than most 4 year olds. He goes to the doctor once a week for a blood test. He receives injections at home. Has high fevers and infections that hospitalize him. We are watching his Marrow closely so he has a Bone Marrow Biopsy done every 6 Months or so. His Neutrophils are unable to get to the site of infection. (Chemostaxis)

85. Shwachman – Diamond Syndrome shwachman – diamond syndrome,, Print this article, shwachman – diamond syndrome,Fig. 1 Pelvis and femora of a boy with shwachman – Diamond syndome. http://www.amershamhealth.com/medcyclopaedia/Volume VII/SHWACHMAN DIAMOND SYNDR

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Shwachman – diamond syndrome, (Harry Shwachman, 20th century, American paediatrician; Louis Diamond, 20th century, American haematologist), (also called metaphyseal chondrodysplasia with exocrine pancreatic insufficiency ), growth retardation, short limb dwarfism, low birth weight, pancreatic insufficiency, malabsorption, recurrent infection and neutropenia. Radiologically, there is mild metaphyseal dysplasia with irregularity of the metaphyses close to the zone of provisional calcification ( Fig.1 ). The pancreas may be shown to be fatty on either MRI or ultrasound. HC The Encyclopaedia of Medical Imaging Volume VII Shwachman – diamond syndrome, Fig. 1

86. The Hospital For Sick Children - Release FOR IMMEDIATE RELEASE December 23, 2002. Sick Kids researchers identifygene for shwachmanDiamond syndrome. You are here Current HSC News. http://www.sickkids.on.ca/mediaroom/custom/sdsgene.asp

Monday, March 31, 2003 Home Find a Career DONATE NOW Media Room ... Foundation HSC Employees Directory The Media Room Home In the News News Release Archive ... News Release Notification Service Backgrounders Media Contacts Media Kit FOR IMMEDIATE RELEASE December 23, 2002 Sick Kids researchers identify gene for Shwachman-Diamond syndrome You are here Current HSC News TORONTO - Researchers at The Hospital for Sick Children (HSC) and the University of Toronto (U of T) have identified the gene that is altered in Shwachman-Diamond syndrome. The researchers studied 250 Shwachman-Diamond syndrome families from around the world and identified two major disease-causing mutations in a gene on chromosome 7. This research is reported in the January issue of the scientific journal Nature Genetics. Shwachman-Diamond syndrome (SDS) is a relatively rare genetic disorder that occurs in approximately one in 50,000 births. SDS affects many organs in the body. Primary features of SDS include a defect in the pancreas that leads to difficulties in digesting food, hematologic (blood) problems with inadequate production of some types of white blood cells, skeletal abnormalities, and short stature. The hematologic problems make people with SDS prone to severe, sometimes fatal infections, and some die from blood complications such as leukemia or bone marrow failure.

87. FUNDING OPPORTUNITY: Shwachman-Diamond Syndrome (SDS)-Canada FUNDING OPPORTUNITY shwachmanDiamond syndrome (SDS)-Canada. SubjectFUNDING OPPORTUNITY shwachman-Diamond syndrome (SDS)-Canada; http://www.sfu.ca/~ors/nserc-list/msg00015.html

Date Prev Date Next Thread Prev Thread Next ... Thread Index FUNDING OPPORTUNITY: Shwachman-Diamond Syndrome (SDS)-Canada To nserc-list@sfu.ca cihr-list@sfu.ca sshrc-list@sfu.ca Subject : FUNDING OPPORTUNITY: Shwachman-Diamond Syndrome (SDS)-Canada From ors@sfu.ca Date : Thu, 15 Feb 2001 15:57:49 -0800 15 FEB 01 The Office of Research Services (ORS) has recently obtained the following information which we are forwarding to list members. ******************* Please note that all applications/proposals/letters of intent must be approved by Research Services using an SFU Research Funding Application Signature Sheet prior to their submission. This form can be found on the website at: http://www.css.sfu.ca/sites/ors/AppSheet.html and must accompany a copy of the application for ORS records. Applicants are strongly advised to allow sufficient lead time for the proper consideration at each level. ******************* AGENCY: Shwachman-Diamond Syndrome (SDS)-Canada PROGRAM: Research Grants TYPES: (i) letter of intent; (ii) application DEADLINES: (i) 15 MAR 02; (ii) 15 MAY 01 (by invitation) See: http://www.shwachman.org

88. Toronto AOII Alumnae Golf Tournament For Shwachman-Diamond Syndrome 3rd Annual Charity Golf Tournament benefiting shwachmanDiamond SyndromeMay 3rd, 2002. The AOII Golf Tournament for shwachman-Diamond http://aoiitoronto.tripod.com/golf2002wrap.htm

d Annual Charity Golf Tournament benefiting Shwachman-Diamond Syndrome May 3rd, 2002 The AOII Golf Tournament for Shwachman-Diamond Syndrome on Friday, May 3rd was a terrific way to end the week with friends, sisters, and of course, golf. Thank you to everyone who came out for golf and/or dinner/auction, and special thanks to our sponsors, volunteers, and Deer Creek. 2003 Sponsors included: Art Gallery of Ontario Bowne Burger King Casa Loma Famous Player's NHLPA Roots Royal Ontario Museum Second City Sports Clubs of Canada Toronto Symphony Orchestra Be sure to keep up on the Alumnae events; there's something for everyone! And if you missed us this year - never fear ~ we'll be back in May 2003!! 2000 AOII Tournament 2001 AOII Tournament A big THANK YOU to our players, diners, auction attendees, volunteers

89. IRSC - Rare Disorders ca Through an educational and informational support network, CEDA is committed tothe enhancement of the lives of all persons affected by EhlersDanlos syndrome http://www.irsc.org:8080/irsc/irscmain.nsf/cat?readform&cat=Rare Disorders&type=

90. Short Description Of Cell Lines. Pathology Shwachman-Bodian Version 4.200205, Short description of cell lines. Pathology shwachmanBodiansyndrome *260400 OMIM record. - By selecting the cell http://www.biotech.ist.unige.it/cldb/pat135.html

91. Stichting Shwachman Syndroom Support Holland Hoe u in het bezit kan komen van meer informatie en wie zijn de bestuursleden? Feitenvan het syndroom en een aantal bruikbare tests voor een goede diagnose. http://www.shwachman.nl/

Hoe u in het bezit kan komen van meer informatie en wie zijn de bestuursleden? Feiten van het syndroom en een aantal bruikbare tests voor een goede diagnose. Links naar andere SSS groepen, en andere relevante onderwerpen. Informatie over onze sponsors en hoe u sponsor kunt worden. Acquisitie stellen wij niet op prijs, sponsoring echter wel. We don't like acquisition, instead we like sponsoring. Dat we zover gekomen zijn hebben we mede te danken aan: 3 maart 2002 Klik hier voor meer informatie over het congres in Verona op 2 en 3 april jl. De volgende bijeenkomst is 8 september aanstaande. Dit wordt een bijeenkomst voor het hele gezin.

92. Wildpuppy's Home Page 3 Our shwachmanDiamond Children. This is one of the captured pictures takenat the shwachman convention in St.Louis this last August 1997. http://members.aol.com/wildpuppy/shwachman.index.html

htmlAdWH('7004944', '120', '30'); htmlAdWH('7002240', '234', '60'); Main Create Edit Help Our Shwachman-Diamond Children Hi, we are Dustin and Ryan from Texas..... My name is Gabriel and I live in Canada. Hi! I'm Katie from Ohio.......... "I'm Ivan, I'm 13 years old, I born in "Catalonian" , it's a state into Spain, in a village near to Barcelona. My hobbies are: the computer games, Roll games. Also, I like drawing very much specially comics if you want to contact with me, send me an email , my address is: tpilar@redestb.es " " Me llamo Ivan, tengo 13 años, He nacido en Cataluña que es un estado dentro de España, en un pueblo cerca de Barcelona. Mis hobys son los juegos de computadora, los juegos de rol y tambien me gusta mucho dibujar, especialmente comics. Si quieres ponerte en contacto conmigo escribeme una email a esta dirección: tpilar@redestb.es " HI ! My name is Brittany and I live in Colorado.... my mom will be replacing this picture as I look awfully tired. My family ask that you keep in your daily prayers right now, as I'm going thur some tough times....

93. Index Of /~sssa Parent Directory 19Jul-20002020 - Apache/1.3.22 Server at home.vicnet.net.au Port 80......Index of /~sssa. Name Last modified Size http://home.vicnet.net.au/~sssa/

Index of /~sssa Name Last modified Size Description ... Parent Directory 19-Jul-2000 20:20 - Apache/1.3.22 Server at home.vicnet.net.au Port 80

94. Pancreatic Elastase-1 Detailed Chronic Pancreatitis, Cystic Fibrosis, Diabetes mellitus, ShwachmanSyndrome and other ailments. EU registration number DE/CA80/7.001. http://www.bioserv-diagnostics.com/gastroenterology/pancreatic_elastase_detailed

Home page up Details on the determination of human fecal pancreatic Elastase-1 with the BIOSERV ELISA For the diagnosis of a pancreatic insufficiency, which may be caused by Chronic Pancreatitis, Cystic Fibrosis, Diabetes mellitus, Shwachman Syndrome and other ailments EU registration number DE/CA80/7.001 Advantages of the BIOSERV ELISA kit for the detecti on of fecal pancreatic elastase-1 in stool p olyclonal antibodies raised against synthetized specific sequences of the human pancreatic Elastase 1 no cross reaction with other human enzymes and other elastases n o cross reaction with pancreatic enzyme substitutes h igh sensitivity and specificity m inimum of strain for patients due to non invasive diagnosis Principle of the test S andwich-ELISA with polyclonal antibodies directed against defined sequences of the human pancreatic elastase-1. Sample material: stool Medical indications for the application of the test E xocrine pancreatic insufficiency , caused by chronic pancreatitis hereditary pancreatitis autoimmunologically caused pancreatitis pancreatic cancer ... Shwachman syndrome C hronic pancreatitis is a progressing disease causing the original and functional pancreatic parenchyma to degenerate in a gradual sclerotic process. Characteristic features are its symptoms (abdominal pain, steatorrhea, loss of weight), typical morphological changes of the

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