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2H Ogier de Baulny

 

Key Opinion Leader In [H Ogier de Baulny is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

  • no keywords assigned

Keywords (17) [keywords assigned to H Ogier de Baulny articles by PubMed, the leading number and the color conveys importance]

  • 2Infant, Newborn | 2Diagnosis, Differential | 2Humans | 1Pentanoic Acids | 1Child | 1Amino Acid Metabolism, Inborn Errors | 1Amino Acids, Branched-Chain | 1Glycine | 1Malonates | 1Maple Syrup Urine Disease | 1Child, Preschool | 1Metabolism, Inborn Errors | 1Propionic Acids | 1Methylmalonic Acid | 1Hematologic Diseases | 1Prognosis | 1Infant

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H Ogier de Baulny Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; H Ogier de Baulny might be a good expert witness on these terms]

  • 7organic | 5aciduria | 4acidurias | 4disorders | 3can | 3orientates | 3anomalies | 3metabolism | 3diseases | 3present | 2mma | 2plasma | 2disease | 2hematologic | 2manifestations | 2urine | 2inborn | 2iva | 2compounds | 2branched-chain | 2anemia | 2abnormality | 2hemolytic | 2pa | 2errors | 2storage | 2lysinuric | 2lysosomal | 2sideroblasts | 2chain | 2symptoms | 2syndrome
  • 4organic acidurias | 2hematologic manifestations | 2errors metabolism | 2anemia orientates | 2inborn errors | 2manifestations inborn | 2branched-chain organic | 2protein intolerance | 2branched chain | 2organic aciduria | 2lysosomal storage | 2storage diseases | 2lysinuric protein | 1diseases organic | 1acidaemia iva | 1aciduria lysosomal | 1compounds using | 1using special | 1severe dehydration | 1pancytopenia orientates | 1commonly encountered | 1lymphohistiocytosis respectively | 1anomalies lysinuric | 1symptoms disorders | 1hypochromia pearson | 1abnormal organic | 1metabolism megaloblastic | 1haematological symptoms | 1vacuolisation precursors | 1group disorders | 1acylcarnitine organic | 1can helpful
  • 2manifestations inborn errors | 2branched-chain organic acidurias | 2inborn errors metabolism | 2hematologic manifestations inborn | 2lysosomal storage diseases | 2lysinuric protein intolerance | 1dehydration leuconeutropenia thrombopenia | 1pearson syndrome sideroblasts | 1organic acidurias branched | 1intolerance lysosomal storage | 1aciduria lysosomal storage | 1anomalies lysinuric protein | 1congenital oroticuria hypochromia | 1diets carnitine branched-chain | 1respectively orientate b12 | 1mma represent commonly | 1group disorders result | 1aciduria lysinuric protein | 1transporter abnormality sideroblasts | 1can diagnosed identifying | 1ketosis ketoacidosis hyperammonaemia | 1absence homocystinuria maple | 1abnormality sideroblasts absence | 1decreased plasma methionine | 1diseases hemolytic anemia | 1thiamine transporter abnormality | 1isoleucine valine mma | 1iva present severe | 1gas chromatography mass | 1precursors thiamine transporter | 1sideroblasts vacuolisation precursors | 1thrombopenia can mimic

Science Trivia (2) [Interactive math & science trivia questions]