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Intrinsic Factor Deficiency
Known as:
IFD
, PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR
National Institutes of Health
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Related topics
Related topics
6 relations
Anemia, Megaloblastic
Autosomal recessive inheritance
Paresthesia
Peripheral Neuropathy
Broader (2)
Anemia, Pernicious
Intrinsic factor
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Evaluation of the diagnostic performance of panfungal polymerase chain reaction assay in invasive fungal diseases
Guojun Cao
,
Z. Xing
,
L. Hua
,
Yu-hua Ji
,
Jia-Bin Sun
,
Zhen Zhao
Experimental and Therapeutic Medicine
2017
Corpus ID: 20520320
Timely diagnosis of invasive fungal diseases (IFDs) is important, as delays in treatment initiation are associated with increased…
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2017
2017
Spectrum of Interface dermatitis : An Observational study'
V. Pawar
,
V. Mane
,
R. Ashtekar
2017
Corpus ID: 59937537
Inroduction: Major role of a dermatopathologists is to try to make specific diagnosis of inflammatory skin diseases. IFD means…
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2017
2017
Methylmalonic Acidemia and Megaloblastic Anemia due to Congenital Intrinsic Factor Deficiency
J. Robles
,
A. Sanchez-Valle
2017
Corpus ID: 40098226
Causes of vitamin B12 deficiency in children include decreased intake, abnormal absorption, and inborn errors of B12 transport…
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2015
2015
Putting CYP2C19 genotyping to the test: utility of pharmacogenomic evaluation in a voriconazole-treated haematology cohort.
Jason A. Trubiano
,
A. Crowe
,
+4 authors
Monica A Slavin
Journal of Antimicrobial Chemotherapy
2015
Corpus ID: 15498367
OBJECTIVES The clinical utility of pharmacogenomic testing in haematology patients with invasive fungal disease (IFD) receiving…
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Review
2012
Review
2012
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
S. M. Tanner
,
A. Sturm
,
E. Baack
,
S. Liyanarachchi
,
A. de la Chapelle
Orphanet Journal of Rare Diseases
2012
Corpus ID: 8664169
BackgroundInherited malabsorption of cobalamin (Cbl) causes hematological and neurological abnormalities that can be fatal. Three…
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2012
2012
Designing of Protein Kinase C β-II Inhibitors against Diabetic complications: Structure Based Drug Design, Induced Fit docking and analysis of active site conformational changes
B. Vijayakumar
,
D. Velmurugan
Bioinformation
2012
Corpus ID: 14877297
Protein Kinase C β-II (PKC β-II) is an important enzyme in the development of diabetic complications like cardiomyopathy…
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2011
2011
Screening Criteria for Diagnosis of Infantile Feeding Disorders as a Cause of Poor Feeding or Food Refusal
A. Levine
,
Lea Bachar
,
+8 authors
M. Boaz
Journal of Pediatric Gastroenterology and…
2011
Corpus ID: 205853835
Objectives:Infantile feeding disorders (IFDs) are a common cause of food refusal, failure to thrive, and vomiting, but they may…
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2011
2011
Selection of an improved HDAC8 inhibitor through structure-based drug design
B. Vijayakumar
,
A. Umamaheswari
,
A. Puratchikody
,
D. Velmurugan
Bioinformation
2011
Corpus ID: 14352731
Histone deacetylases (HDACs) are enzymes, which catalyze the removal of acetyl moiety from acetyl-lysine within the histone…
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2009
2009
Consideraciones prácticas sobre las curvas IFD
Y. R. López
,
N. M. León
,
A. L. Méndez
2009
Corpus ID: 194143229
Se aborda el procesamiento de las lluvias maximas para la confeccion de las curvas de intensidad, duracion y frecuencia de…
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2008
2008
[Hereditary juvenile cobalamin deficiency due to mutations in GIF gene].
M. C. García Jiménez
,
A. Baldellóu Vázquez
,
M. T. Calvo Martín
,
G. Pérez-Lungmus
,
J. López Pisón
Anales de Pediatría
2008
Corpus ID: 37115415
Inborn errors of cobalamin (Cbl) metabolism affect its absorption, transport, as well as its intracellular metabolism. Hereditary…
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