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Lipoamide dehydrogenase deficiency: A new cause for recurrent myoglobinuria
被引:0
作者
:
Elpeleg, ON
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Elpeleg, ON
Saada, AB
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Saada, AB
Shaag, A
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Shaag, A
Glustein, JZ
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Glustein, JZ
Ruitenbeek, W
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Ruitenbeek, W
Tein, I
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Tein, I
Halevy, J
论文数:
0
引用数:
0
h-index:
0
机构:
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
Halevy, J
机构
:
[1]
SHAARE ZEDEK MED CTR, INTERNAL MED UNIT, IL-91031 JERUSALEM, ISRAEL
[2]
UNIV NIJMEGEN HOSP, DEPT PEDIAT, NL-6500 HB NIJMEGEN, NETHERLANDS
[3]
HOSP SICK CHILDREN, DIV NEUROL, TORONTO, ON M5G 1X8, CANADA
来源
:
MUSCLE & NERVE
|
1997年
/ 20卷
/ 02期
关键词
:
lactic acidemia;
myoglobinuria;
lipoamide dehydrogenase deficiency;
D O I
:
暂无
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
引用
收藏
页码:238 / 240
页数:3
相关论文
共 35 条
[1]
Lipoamide dehydrogenase deficiency:: a newly discovered cause of acute hepatitis in adults
Barak, N
论文数:
0
引用数:
0
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0
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Beilinson Hosp, Rabin Med Ctr, Dept Med D, IL-49100 Petah Tiqwa, Israel
Barak, N
Huminer, D
论文数:
0
引用数:
0
h-index:
0
机构:
Beilinson Hosp, Rabin Med Ctr, Dept Med D, IL-49100 Petah Tiqwa, Israel
Huminer, D
Segal, T
论文数:
0
引用数:
0
h-index:
0
机构:
Beilinson Hosp, Rabin Med Ctr, Dept Med D, IL-49100 Petah Tiqwa, Israel
Segal, T
Ben Ari, Z
论文数:
0
引用数:
0
h-index:
0
机构:
Beilinson Hosp, Rabin Med Ctr, Dept Med D, IL-49100 Petah Tiqwa, Israel
Ben Ari, Z
Halévy, J
论文数:
0
引用数:
0
h-index:
0
机构:
Beilinson Hosp, Rabin Med Ctr, Dept Med D, IL-49100 Petah Tiqwa, Israel
Halévy, J
Kaspa, RT
论文数:
0
引用数:
0
h-index:
0
机构:
Beilinson Hosp, Rabin Med Ctr, Dept Med D, IL-49100 Petah Tiqwa, Israel
Kaspa, RT
JOURNAL OF HEPATOLOGY,
1998,
29
(03)
: 482
-
484
[2]
Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews
Shaag, A
论文数:
0
引用数:
0
h-index:
0
机构:
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Shaag, A
Saada, A
论文数:
0
引用数:
0
h-index:
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Berger, I
论文数:
0
引用数:
0
h-index:
0
机构:
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Mandel, H
论文数:
0
引用数:
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h-index:
0
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Mandel, H
Joseph, A
论文数:
0
引用数:
0
h-index:
0
机构:
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Joseph, A
Feigenbaum, A
论文数:
0
引用数:
0
h-index:
0
机构:
Shaare Zedek Med Ctr, Metab Dis Unit, IL-91031 Jerusalem, Israel
Feigenbaum, A
Elpeleg, ON
论文数:
0
引用数:
0
h-index:
0
机构:
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Shaare Zedek Med Ctr, Metab Dis Unit, IL-91031 Jerusalem, Israel
Elpeleg, ON
AMERICAN JOURNAL OF MEDICAL GENETICS,
1999,
82
(02):
: 177
-
182
[3]
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria
Minetti, C
论文数:
0
引用数:
0
h-index:
0
机构:
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Minetti, C
Garavaglia, B
论文数:
0
引用数:
0
h-index:
0
机构:
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Garavaglia, B
Bado, M
论文数:
0
引用数:
0
h-index:
0
机构:
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论文数:
0
引用数:
0
h-index:
0
机构:
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Bruno, C
论文数:
0
引用数:
0
h-index:
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Rimoldi, M
论文数:
0
引用数:
0
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引用数:
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0
引用数:
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引用数:
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NEUROMUSCULAR DISORDERS,
1998,
8
(01)
: 3
-
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[4]
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhood
de Lonlay-Debeney, P
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France
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Edery, P
论文数:
0
引用数:
0
h-index:
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引用数:
0
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30
(01)
: 42
-
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[5]
CYTOCHROME-C-OXIDASE DEFICIENCY PRESENTING AS RECURRENT NEONATAL MYOGLOBINURIA
SAUNIER, P
论文数:
0
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CHRETIEN, D
论文数:
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ROTIG, A
BONNEFONT, JP
论文数:
0
引用数:
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论文数:
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RUSTIN, P
NEUROMUSCULAR DISORDERS,
1995,
5
(04)
: 285
-
289
[6]
Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: Expression of the molecular phenotype in cultured muscle cells
Villard, J
论文数:
0
引用数:
0
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0
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Fischer, A
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0
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引用数:
0
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引用数:
0
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引用数:
0
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0
机构:
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JOURNAL OF THE NEUROLOGICAL SCIENCES,
1996,
136
(1-2)
: 178
-
181
[7]
Necrotizing Vacuolar Myopathy Presenting with Recurrent Myoglobinuria
Nandhagopal, Ramachandiran
论文数:
0
引用数:
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INTERNATIONAL JOURNAL OF NEUROSCIENCE,
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120
(12)
: 784
-
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[8]
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CHIADOPIAT, L
论文数:
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引用数:
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h-index:
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论文数:
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引用数:
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h-index:
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机构:
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论文数:
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引用数:
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h-index:
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JOURNAL OF NEUROLOGY,
1991,
238
(06)
: 323
-
324
[9]
Very-long-chain acyl-coenzyme A dehydrogenase deficiency - a new cause of myoglobinuric acute renal failure
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论文数:
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引用数:
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NEPHROLOGY DIALYSIS TRANSPLANTATION,
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15
(08)
: 1232
-
1234
[10]
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria
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NEUROPEDIATRICS,
2002,
33
(02)
: 109
-
111
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