Hugo W. Moser - Publications, H-index & Citations

Hugo W. Moser

Johns Hopkins University

77H指数

450论文数

2.0W被引数

收录论文 49

发表时间

PEX12, the pathogenic gene of group III Zellweger syndrome:: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of Pex12p

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-28

OAAI

Okumoto, K; Shimozawa, N; Kawai, A; Tamura, S; Tsukamoto, T; Osumi, T; Moser, H; Wanders, RJA; Suzuki, Y; Kondo, N; Fujiki, Y

Human and great ape red blood cells differ in plasmalogen levels and composition

LIPIDS IN HEALTH AND DISEASE

IF4.2

2011-06-17

OAAI

Moser, Ann B.; Steinberg, Steven J.; Watkins, Paul A.; Moser, Hugo W.; Ramaswamy, Krishna; Siegmund, Kimberly D.; Lee, D. Rick; Ely, John J.; Ryder, Oliver A.; Hacia, Joseph G.

SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2011-01-12

OAAI

Schlotawa, Lars; Ennemann, Eva Charlotte; Radhakrishnan, Karthikeyan; Schmidt, Bernhard; Chakrapani, Anupam; Christen, Hans-Juergen; Moser, Hugo; Steinmann, Beat; Dierks, Thomas; Gaertner, Jutta

Identification of Novel Mutations and Sequence Variation in the Zellweger Syndrome Spectrum of Peroxisome Biogenesis Disorders

HUMAN MUTATION

IF3.7

2009-03-01

OAAI

Yik, Wing Yan; Steinberg, Steven J.; Moser, Ann B.; Moser, Hugo W.; Hacia, Joseph G.

Quantitative Magnetization Transfer Characteristics of the Human Cervical Spinal Cord In Vivo: Application to Adrenomyeloneuropathy

MAGNETIC RESONANCE IN MEDICINE

IF3

2008-12-18

OAAI

Smith, Seth A.; Golay, Xavier; Fatemi, Ali; Mahmood, Asif; Raymond, Gerald V.; Moser, Hugo W.; van Zijl, Peter C. M.; Stanisz, Greg J.

Auditory function in adrenomyeloneuropathy

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2008-06-01

OAAI

Pillion, Joseph P.; Moser, Hugo W.; Raymond, Gerald V.

Peroxisomal disorders: Overview

PEROXISOMES: BIOLOGY AND ROLE IN TOXICOLOGY AND DISEASE

IF0

2006-12-17

PREAI

Moser, HW; Moser, AB

Expression of ALDP is altered in X-linked adrenoleukodystrophy

PEROXISOMES: BIOLOGY AND ROLE IN TOXICOLOGY AND DISEASE

IF0

2006-12-17

PREAI

Watkins, PA; Gould, SJ; Smith, MA; Braiterman, LT; Wei, HM; Kok, F; Moser, AB; Moser, HW; Smith, KD

Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p•Pex6p complex

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2006-01-01

OAAI

Furuki, S; Tamura, S; Matsumoto, N; Miyata, N; Moser, A; Moser, HW; Fujiki, Y

Adrenoleukodystrophy - New approaches to a neurodegenerative disease

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

IF55

2005-12-28

113

PREAI

Moser, HW; Raymond, GV; Dubey, P

Adreno-leukodystrophy: Oxidative stress of mice and men

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

IF3

2005-12-01

114

OAAI

Powers, JM; Pei, ZT; Heinzer, AK; Deering, R; Moser, AB; Moser, HW; Watkins, PA; Smith, KD

Progressive cavitating leukoencephalopathy: A novel childhood disease

ANNALS OF NEUROLOGY

IF7.7

2005-11-28

OAAI

Naidu, S; Bibat, G; Lin, D; Burger, P; Barker, P; Rosemberg, S; Braverman, N; Arroyo, H; Dowling, M; Hamosh, A; Kimonis, V; Blank, C; Fiumara, A; Facchini, S; Singhal, B; Moser, H; Kelley, R; DiMauro, S

Diffusion tensor-based imaging reveals occult abnormalities in adrenomyeloneuropathy

ANNALS OF NEUROLOGY

IF7.7

2005-10-20

PREAI

Dubey, P; Fatemi, A; Huang, H; Nagae-Poetscher, L; Wakana, S; Barker, PB; van Zijl, P; Moser, HW; Mori, S; Raymond, GV

Adrenal insufficiency in asymptomatic adrenoleukodystrophy patients identified by very long-chain fatty acid screening

JOURNAL OF PEDIATRICS

IF3.5

2005-04-01

110

PREAI