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DISCUSSION OF "LATE WISCONSINAN MOUNTAIN GLACIATION IN THE NORTHERN PRESIDENTIAL RANGE, NEW HAMPSHIRE" BY DWIGHT C. BRADLEY = DISCUSSION A PROPOS DE LA GLACIATION DE MONTAGNE DU WISCONSINIEN SUP DANS LA CHAINE PRESIDENTIAL SEPTENTRIONALE, NEW HAMPSHIREGERATH ROBERT F; FOWLER BRIAN K.1982; ARCT. ALP. RES.; ISSN 0004-0851; USA; DA. 1982-11; VOL. 14; NO 4; PP. 369-370; BIBL. 11 REF.Article

STRUCTURAL GEOLOGIC AND ROCK MECHANICS CONSIDERATIONS IN SITING CRUSHED STONE QUARRIES IN VERMONT = CONSIDERATIONS DE GEOLOGIE STRUCTURALE ET DE MECANIQUE DES ROCHES POUR SITUER L'EMPLACEMENT DE CARRIERES DE ROCHES CONCASSEES DANS LE VERMONTFOWLER BRIAN K; DETENBECK JC ED.1981; GREEN MT. GEOL.; ISSN 0271-0102; USA; DA. 1981; VOL. 7; NO 4; PP. 17Conference Paper

Clinical and molecular studies of mitochondrial diseaseGOTO, Y.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 181-188, issn 0141-8955Conference Paper

Enzyme replacement therapy in mucopolysaccharidosis type I : Progress and emerging difficultiesWRAITH, J. E.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 245-250, issn 0141-8955Conference Paper

Enzyme replacement and beyondDESNICK, R. J.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 251-265, issn 0141-8955Conference Paper

Frequency interference artifactFOWLER, Brian C; KOLLURI, Raghu.Vascular medicine (London). 2011, Vol 16, Num 4, pp 312-313, issn 1358-863X, 2 p.Article

Liver repopulation for the treatment of metabolic diseasesGROMPE, M.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 231-244, issn 0141-8955Conference Paper

Rare diseases and the assessment of intervention : What sorts of clinical trials can we use?WILCKEN, B.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 291-298, issn 0141-8955Conference Paper

Changes in clinical practice with the unravelling of diseases : Connective-tissue disordersSPRANGER, J.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 117-126, issn 0141-8955Conference Paper

Garrod's foresight; our hindsightSCRIVER, C. R.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 93-116, issn 0141-8955Conference Paper

Newborn mass screening versus selective investigation : Benefits and costsPOLLITT, R. J.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 299-302, issn 0141-8955Conference Paper

Applications of mass spectrometry in the study of inborn errors of metabolismCLAYTON, P. T.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 139-150, issn 0141-8955Conference Paper

Comparing Clinical Characteristics Between Hospitalized Adults With Laboratory-Confirmed Influenza A and B Virus InfectionSU SU; CHAVES, Sandra S; MORIN, Craig et al.Clinical infectious diseases. 2014, Vol 59, Num 2, pp 252-255, issn 1058-4838, 4 p.Article

A novel mutation in LMBRD1 causes the cblF defect of vitamin B₁₂ metabolism in a Turkish patientGAILUS, Susann; SUORMALA, Terttu; MALERCZYK-AKTAS, Ayse Gül et al.Journal of inherited metabolic disease. 2010, Vol 33, Num 1, pp 17-24, issn 0141-8955, 8 p.Article

Identification of a novel PCB source through analysis of 209 PCB congeners by US EPA modified method 1668LITTEN, Simon; FOWLER, Brian; LUSZNIAK, Diane et al.Chemosphere (Oxford). 2002, Vol 46, Num 9-10, pp 1457-1459, issn 0045-6535Conference Paper

A structural hypothesis for BH₄ responsiveness in patients with mild forms of hyperphenylalaninaemia and phenylketonuriaERLANDSEN, H; STEVENS, R. C.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 213-230, issn 0141-8955Conference Paper

The use of functional genomics in C. elegans for studying human development and diseaseKUWABARA, P. E; O'NEIL, N.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 127-138, issn 0141-8955Conference Paper

Asacol^®-induced Neutropenia Resolution Without the Use of Granulocyte Colony-stimulating FactorFOWLER, Brian T; GUPTA, Tina; BILAL, Muhammad et al.Southern medical journal (Birmingham, Ala. Print). 2010, Vol 103, Num 11, pp 1167-1169, issn 0038-4348, 3 p.Article

Import of proteins into mitochondria : A novel pathomechanism for progressive neurodegenerationBAUER, M. F; NEUPERT, W.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 166-180, issn 0141-8955Conference Paper

Diagnosis of mitochondrial disorders : Clinical and biochemical approachTHORBURN, D. R; SMEITINK, J.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 312-316, issn 0141-8955Conference Paper

LMBRD1: the gene for the cblF defect of vitamin B₁₂ metabolism : HOMOCYSTEINE AND B-VITAMIN METABOLISMRUTSCH, Frank; GAILUS, Susann; SUORMALA, Terttu et al.Journal of inherited metabolic disease. 2011, Vol 34, Num 1, pp 121-126, issn 0141-8955, 6 p.Article

5, 10-Methylenetetrahydrofolate reductase (MTHFR) Assay in the forward direction: Residual activity in MTHFR deficiencySUORMALA, Terttu; GAMSE, Gertraud; FOWLER, Brian et al.Clinical chemistry (Baltimore, Md.). 2002, Vol 48, Num 6, pp 835-843, issn 0009-9147, 1Article

Prenatal and postnatal treatment in cobalamin C defectHUEMER, Martina; SIMMA, Burkhard; FOWLER, Brian et al.The Journal of pediatrics. 2005, Vol 147, Num 4, pp 469-472, issn 0022-3476, 4 p.Article

Biotin-dependent carboxylase activities in different CNS and skin-derived cells, and their sensitivity to biotin-depletionSUORMALA, Terttu; WIESMANN, Ulrich N; CRUZ, Fatima et al.International journal for vitamin and nutrition research. 2002, Vol 72, Num 4, pp 278-286, issn 0300-9831Article