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genetic or congenital, metabolic, nephrology
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primary hyperoxaluria - increased blood oxalate causing kidney stones
Definition for primary hyperoxaluria
Primary hyperoxaluria is a rare condition characterized by the overproduction of a substance called oxalate (or oxalic acid).
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Primary hyperoxaluria is a rare condition characterized by the overproduction of a substance called oxalate (or oxalic acid). In the kidneys, the excess oxalate combines with calcium to form calcium oxalate, a hard compound that is the main component of kidney stones. Deposits of calcium oxalate can lead to kidney damage, kidney failure, and injury to other organs.
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some common symptoms
high blood pressure
painful urination in females
swollen feet and legs
urinating less than normal
some related diagnoses
1 - 7 of
79
diagnoses
acute renal failure
acute tubular necrosis
urinary tract obstruction
lupus nephritis
cystinuria
renal artery occlusion
membranoproliferative glomerulonephritis
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do i have 'primary hyperoxaluria'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'primary hyperoxaluria'
1 - 5 of
26
diagnostic tests
24-hour urine oxalate
primary hyperoxaluria and 24-hour urine oxalate
Molecular Genetic Studies
primary hyperoxaluria and Molecular Genetic Studies
BUN
primary hyperoxaluria and BUN
Dietary questionnaire
primary hyperoxaluria and Dietary questionnaire
KUB
primary hyperoxaluria and KUB
Serum Creatinine
primary hyperoxaluria and Serum Creatinine
Serum calcium
primary hyperoxaluria and Serum calcium
Ultrasonography kidneys ureter bladder
primary hyperoxaluria and Ultrasonography kidneys ureter bladder
Urinalysis
Examination of urine to detect disease
primary hyperoxaluria and Urinalysis
spiral CT urinary tract
primary hyperoxaluria and spiral CT urinary tract
24 hour urine magnesium
the amount of magnesium that is excreted from the body
primary hyperoxaluria and 24 hour urine magnesium
24 hour urine potassium
the amount of potassium that is excreted from the body
primary hyperoxaluria and 24 hour urine potassium
24-hour urine creatinine
primary hyperoxaluria and 24-hour urine creatinine
24-hour urine uric acid
primary hyperoxaluria and 24-hour urine uric acid
24-hour urine volume
primary hyperoxaluria and 24-hour urine volume
24-hour urine phosphate
primary hyperoxaluria and 24-hour urine phosphate
urinary citrate
primary hyperoxaluria and urinary citrate
urine pH
primary hyperoxaluria and urine pH
24-hour urine calcium
primary hyperoxaluria and 24-hour urine calcium
24-hour urine for oxalate
primary hyperoxaluria and 24-hour urine for oxalate
24-hour urine sodium
primary hyperoxaluria and 24-hour urine sodium
Biopsy liver
primary hyperoxaluria and Biopsy liver
Diet diary
primary hyperoxaluria and Diet diary
Spiral CT
primary hyperoxaluria and Spiral CT
Urinary electrolytes
primary hyperoxaluria and Urinary electrolytes
serum oxalate
primary hyperoxaluria and serum oxalate
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therapeutic procedures for 'primary hyperoxaluria'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for primary hyperoxaluria:
therapeutic procedure search results for 'primary hyperoxaluria'
1 - 5 of
9
therapeutic procedures
rankings are computer generated. please consult your health care provider.
Increasing urinary volume
primary hyperoxaluria and Increasing urinary volume
liver-kidney transplantation
primary hyperoxaluria and liver-kidney transplantation
low-oxalate diet
primary hyperoxaluria and low-oxalate diet
reduced meat-protein
primary hyperoxaluria and reduced meat-protein
Intensive dialysis
primary hyperoxaluria and Intensive dialysis
Dialysis
primary hyperoxaluria and Dialysis
Nutritional counseling
primary hyperoxaluria and Nutritional counseling
diet modification
primary hyperoxaluria and diet modification
low fat diet
primary hyperoxaluria and low fat diet
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medications search results for 'primary hyperoxaluria'
1 - 5 of
7
medications
rankings are computer generated. please consult your health care provider.
pyridoxine
primary hyperoxaluria and pyridoxine
Potassium phosphate and sodium phophate
primary hyperoxaluria and Potassium phosphate and sodium phophate
hydrochlorothiazide
primary hyperoxaluria and hydrochlorothiazide
Oxalobacter formigenes
primary hyperoxaluria and Oxalobacter formigenes
Orthophosphate
primary hyperoxaluria and Orthophosphate
Magnesium oxide
primary hyperoxaluria and Magnesium oxide
pentosan polysulfate
primary hyperoxaluria and pentosan polysulfate
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web search results for primary hyperoxaluria
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1 - 50
- primary hyperoxaluria
Primary hyperoxaluria - Wikipedia, the free encyclopedia
Primary hyperoxaluria results in increased excretion of oxalate, with oxalate ... Primary hyperoxaluria, on the other hand, refers to a specific type of ...
http://en.wikipedia.org/wiki/Primary_hyperoxaluria
en.wikipedia.org
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summary
Primary hyperoxaluria - Genetics Home Reference
Primary hyperoxaluria is a rare condition characterized by the overproduction of ... Mutations in the AGXT and GRHPR genes cause primary hyperoxaluria. ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria
ghr.nlm.nih.gov
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Primary Hyperoxaluria Type 1 -- GeneReviews -- NCBI Bookshelf
In primary hyperoxaluria type 1, supersaturation of the urine with oxalate leads ... Primary hyperoxaluria was first described in the 1920s but not recognized as a ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ph1
www.ncbi.nlm.nih.gov
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summary
Primary hyperoxaluria - OMIM - Genetic disorder catalog - Genetics Home ...
... in the Genetics Home Reference condition summary on primary hyperoxaluria. OMIM topic: Hyperoxaluria, primary, type I. OMIM topic: Hyperoxaluria, primary, type II ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/OMIM
ghr.nlm.nih.gov
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Primary Hyperoxaluria Type 2 -- GeneReviews -- NCBI Bookshelf
The age of onset of primary hyperoxaluria type 2 (PH2) is typically in childhood ... Primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ph2
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria - Patient support - For patients and families ...
Genetic Conditions > primary hyperoxaluria > Patient support - For patients and ... in the Genetics Home Reference condition summary on primary hyperoxaluria. ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Patient+support
ghr.nlm.nih.gov
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summary
Gene symbol: AGXT. Disease: primary hyperoxaluria type I.
1: Hum Genet. 1999 May;104(5):441. Gene symbol: AGXT. Disease: primary hyperoxaluria type I. ... Hyperoxaluria, Primary/classification. Hyperoxaluria, Primary ...
http://www.ncbi.nlm.nih.gov/pubmed/10394939
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria - References - Genetics Home Reference
Molecular aetiology of primary hyperoxaluria type 1. Nephron Exp Nephrol. ... D, Marangella M, Amoroso A. Primary hyperoxaluria: genotype-phenotype correlation. ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/References
ghr.nlm.nih.gov
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summary
Primary hyperoxaluria type 1 in Japan.
Primary hyperoxaluria type 1 in Japan. Ichiyama A, Oda T, Maeda-Nakai E. ... missing as in the case of primary hyperoxaluria type 1 (PH1) more glyoxylate is ...
http://www.ncbi.nlm.nih.gov/pubmed/11330044?ordinalpos=2&ito...
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria - Related Gene(s) - Genetics Home Reference
Genetic Conditions > primary hyperoxaluria > Related Gene(s) ... Lister Hill National Center for Biomedical Communications ... Department of Health & Human ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Related+Gene(s)
ghr.nlm.nih.gov
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summary
Primary hyperoxaluria type 2 in children.
Primary hyperoxaluria type 2 in children. Johnson SA, Rumsby G, Cregeen D, Hulton SA. ... The primary hyperoxalurias (PH1 and PH2) are rare defects of oxalate ...
http://www.ncbi.nlm.nih.gov/pubmed/12185464
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria - Educational resources - Information pages ...
... in the Genetics Home Reference condition summary on primary hyperoxaluria. Ask the Geneticist: Inheritance of Primary Hyperoxaluria. Madisons Foundation ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Educational+resources
ghr.nlm.nih.gov
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Primary hyperoxaluria.
... Electrolyte Metab. 1994;20(6):340-51. Primary hyperoxaluria. Scheinman JI. ... Primary hyperoxaluria (PH) is a rare inborn error of amino acid metabolism, now ...
http://www.ncbi.nlm.nih.gov/pubmed/7783696
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria - Gene Reviews - Clinical summary - Genetics Home ...
... in the Genetics Home Reference condition summary on primary hyperoxaluria. Gene Review: Primary Hyperoxaluria, Type 1. Gene Review: Primary Hyperoxaluria, Type 2 ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Gene+Reviews
ghr.nlm.nih.gov
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summary
Primary hyperoxaluria - MedlinePlus - Health information - Genetics ...
Genetic Conditions > primary hyperoxaluria > MedlinePlus - Health information ... in the Genetics Home Reference condition summary on primary hyperoxaluria. ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/MedlinePlus
ghr.nlm.nih.gov
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Primary hyperoxaluria type 1 in Japan.
Primary hyperoxaluria type 1 in Japan. Takayama T, Nagata M, Ichiyama A, Ozono S. ... AIMS: Current status of primary hyperoxaluria (PH) has not been surveyed ...
http://www.ncbi.nlm.nih.gov/pubmed/15961950?ordinalpos=1&ito...
www.ncbi.nlm.nih.gov
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Molecular etiology of primary hyperoxaluria type 1: new directions for ...
Molecular etiology of primary hyperoxaluria type 1: new directions for treatment. ... Primary hyperoxaluria type 1 (PH1) is a rare autosomal-recessive disorder caused ...
http://www.ncbi.nlm.nih.gov/pubmed/15961951
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria - Additional NIH Resources - National Institutes ...
... primary hyperoxaluria > ... Home Reference condition summary on primary hyperoxaluria. ... National Institute of Diabetes and Digestive and Kidney ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/A...
ghr.nlm.nih.gov
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Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of ...
Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the ... Primary hyperoxaluria type 1 (PH1) is a severe autosomal recessive inborn error ...
http://www.ncbi.nlm.nih.gov/pubmed/9192270
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria
Primary hyperoxaluria type 1is a rare metabolic disorder transmitted as an ... Primary hyperoxaluria, calcium-oxalate deposition, Glyoxalate, L-alanine: ...
http://www.orpha.net/data/patho/GB/uk-oxalos.pdf
www.orpha.net
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summary
Hyperoxaluria, Primary (Type I) - Yahoo! Health
Important It is possible that the main title of the report Hyperoxaluria, Primary (Type I) is not the name you expected. Please check the synonyms listing to find ...
http://health.yahoo.com/urinary-overview/hyperoxaluria-prima...
health.yahoo.com
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Primary hyperoxaluria type I due to a point mutation of T to C in the ...
Primary hyperoxaluria type I due to a point mutation of T to C in the coding ... constructed from the liver of a primary hyperoxaluria type I (PH1) case in which ...
http://www.ncbi.nlm.nih.gov/pubmed/2039493
www.ncbi.nlm.nih.gov
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Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion ...
Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of ... with the autosomal recessive disease primary hyperoxaluria type 1, there is a ...
http://www.ncbi.nlm.nih.gov/pubmed/8507692
www.ncbi.nlm.nih.gov
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Liver transplantation for type 1 primary hyperoxaluria as a cure for ...
Liver transplantation for type 1 primary hyperoxaluria as a cure for combined thrombophilia. ... Hyperoxaluria, Primary/surgery* Kidney Transplantation. Liver ...
http://www.ncbi.nlm.nih.gov/pubmed/15543348?ordinalpos=15&it...
www.ncbi.nlm.nih.gov
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Oxalosis and Hyperoxaluria
This information is provided as a resource and does not constitute an ... professionals in the field of primary hyperoxaluria and oxalate stone disease. ...
http://www.webmd.com/a-to-z-guides/oxalosis-and-hyperoxaluria
www.webmd.com
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Talk:Primary hyperoxaluria - Wikipedia, the free encyclopedia
Talk:Primary hyperoxaluria. From Wikipedia, the free encyclopedia. Jump to: navigation, search. This article is within the scope of WikiProject Medicine. ...
http://en.wikipedia.org/wiki/Talk:Primary_hyperoxaluria
en.wikipedia.org
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Kidney Stones
Hyperoxaluria is defined as either primary or secondary. Primary hyperoxaluria is an inherited disorder in which excess oxalate in the ...
http://adam.about.com/reports/000081_2.htm
adam.about.com
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Oxalosis - NextBio
Oxalosis in primary hyperoxaluria in infancy : Report of a case in a 3-month-old ... Primary hyperoxaluria (PH1) is a rare inborn autosomal recessive metabolic ...
http://www.nextbio.com/b/home/home.nb?q=oxalosis
www.nextbio.com
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Tubulointerstitial Nephritis: Tubulointerstitial Diseases: Merck Manual ...
Tubulointerstitial nephritis can be primary or can be secondary to glomerular ... (types I and II primary hyperoxaluria) or acquired GI diseases (eg, short bowel ...
http://www.merck.com/mmpe/sec17/ch236/ch236c.html
www.merck.com
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Oxalosis and Hyperoxaluria - Yahoo! Health
... professionals in the field of primary hyperoxaluria and oxalate stone disease. ... Oxalosis and Hyperoxaluria Fdn. 201 East 19th Street, #12E. New York, NY 10003 ...
http://health.yahoo.com/urinary-resources/oxalosis-and-hyper...
health.yahoo.com
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Kidney stones
Hyperoxaluria can be either primary or secondary. Primary hyperoxaluria is an inherited disorder in which too much oxalate in the ...
http://adam.about.com/reports/Kidney-stones.htm
adam.about.com
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New York Methodist Hospital
Hyperoxaluria can be either primary or secondary. Primary hyperoxaluria is an inherited disorder in which too much oxalate in the ...
http://nymethodist.adam.com/content.aspx?productId=10&pid=10&gid=000081
nymethodist.adam.com
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Primary hyperoxaluria - Gene Tests - DNA tests ordered by healthcare ...
Genetic Conditions > primary hyperoxaluria > ... on primary hyperoxaluria. Gene Tests: Hyperoxaluria, Primary, Type 1. Gene Tests: Hyperoxaluria, Primary, Type ...
http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Gene+Tests
ghr.nlm.nih.gov
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AGXT - alanine-glyoxylate aminotransferase - Genetics Home Reference
primary hyperoxaluria - caused by mutations in the AGXT gene ... As a result, glyoxylate accumulates, leading to the signs and symptoms of primary hyperoxaluria. ...
http://ghr.nlm.nih.gov/gene=agxt
ghr.nlm.nih.gov
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A United States survey on diagnosis, treatment, and outcome of primary ...
A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluria. ... Primary hyperoxaluria (PH) is a heterogeneous disease with a variable age of ...
http://www.ncbi.nlm.nih.gov/pubmed/12920626
www.ncbi.nlm.nih.gov
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AGXT - References - Genetics Home Reference
Preliminary Evidence for Ethnic Differences in Primary Hyperoxaluria Type 1 Genotype. ... Molecular aetiology of primary hyperoxaluria type 1. Nephron Exp Nephrol. ...
http://ghr.nlm.nih.gov/gene=agxt/show/References
ghr.nlm.nih.gov
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Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to ...
In approximately one-third of primary hyperoxaluria type 1 patients, disease is ... with reference to the AGT targeting defect in primary hyperoxaluria and also ...
http://www.ncbi.nlm.nih.gov/pubmed/1961759
www.ncbi.nlm.nih.gov
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The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in ...
... reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II. ... Primary hyperoxaluria type II (PH2) is a rare monogenic disorder that is ...
http://www.ncbi.nlm.nih.gov/pubmed/10484776
www.ncbi.nlm.nih.gov
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Food, nutrition, and metabolism - Genetics Home Reference
D-glycerate dehydrogenase deficiency see primary hyperoxaluria ... glyceric aciduria see primary hyperoxaluria. glycine encephalopathy ...
http://ghr.nlm.nih.gov/conditionCategory=foodnutritionandmetabolism
ghr.nlm.nih.gov
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Diagnostic and therapeutic approaches in patients with secondary ...
Secondary hyperoxaluria is due either to increased intestinal oxalate absorption ... urinary oxalate excretion is usually lower than in primary hyperoxaluria, it may ...
http://www.ncbi.nlm.nih.gov/pubmed/12957811
www.ncbi.nlm.nih.gov
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Hyperoxaluria - Wikipedia, the free encyclopedia
A child with primary hyperoxaluria was treated with a liver and kidney transplant.[2] ... "Primary hyperoxaluria - Genetics Home Reference" ...
http://en.wikipedia.org/wiki/Hyperoxaluria
en.wikipedia.org
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GRHPR - glyoxylate reductase/hydroxypyruvate reductase - Genetics Home ...
primary hyperoxaluria - caused by mutations in the GRHPR gene ... more than a dozen GRHPR mutations that cause type 2 primary hyperoxaluria. ...
http://ghr.nlm.nih.gov/gene=grhpr
ghr.nlm.nih.gov
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Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary ...
Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I. ... that primary hyperoxaluria type I should be added to the rather ...
http://www.ncbi.nlm.nih.gov/pubmed/3709805
www.ncbi.nlm.nih.gov
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GRHPR - References - Genetics Home Reference
... metabolism: implications for primary hyperoxaluria. Am J Nephrol. ... Pirulli D, Marangella M, Amoroso A. Primary hyperoxaluria: genotype-phenotype correlation. ...
http://ghr.nlm.nih.gov/gene=grhpr/show/References
ghr.nlm.nih.gov
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Enzymological and mutational analysis of a complex primary ...
... analysis of a complex primary hyperoxaluria type 1 phenotype involving ... Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease caused ...
http://www.ncbi.nlm.nih.gov/pubmed/8101040
www.ncbi.nlm.nih.gov
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Should liver transplantation be performed before advanced renal ...
Primary hyperoxaluria type 1 (PH1) is a rare recessive autosomal inborn error of ... Hyperoxaluria, Primary/complications* Kidney Failure, Chronic/diagnosis ...
http://www.ncbi.nlm.nih.gov/pubmed/8476723
www.ncbi.nlm.nih.gov
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Genomics|HuGENet|Literature|2007 May 3
The mission of the National Office of Public Health Genomics is to integrate advances in human genetics into ... 1 Primary Hyperoxaluria Shows Feasibility ...
http://www.cdc.gov/genomics/hugenet/literature/2007/Hmay03.htm
www.cdc.gov
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Kidneys and urinary system - Genetics Home Reference
D-glycerate dehydrogenase deficiency see primary hyperoxaluria ... primary hyperoxaluria. Primary hyperuricemia syndrome see Lesch-Nyhan syndrome ...
http://ghr.nlm.nih.gov/conditionCategory=kidneysandurinarysystem
ghr.nlm.nih.gov
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Identification of missense, nonsense, and deletion mutations in the ...
... mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2) ... Primary hyperoxaluria type II (PH2) is a rare disease characterized by the ...
http://www.ncbi.nlm.nih.gov/pubmed/11030416
www.ncbi.nlm.nih.gov
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A glycine-to-glutamate substitution abolishes alanine:glyoxylate ...
... catalytic activity in a subset of patients with primary hyperoxaluria type 1. ... primary hyperoxaluria type 1 (PH1) patient who had normal levels of hepatic ...
http://www.ncbi.nlm.nih.gov/pubmed/1349575
www.ncbi.nlm.nih.gov
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