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Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2: causative or consequential?
被引:30
作者
:
Schneider, S. A.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lubeck, Dept Neurol, Schilling Dept Clin & Mol Neurogenet, Lubeck, Germany
UCL, Sobell Dept, Inst Neurol, London WC1N 3BG, England
Schneider, S. A.
[
2
]
Hardy, J.
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Sobell Dept, Inst Neurol, London WC1N 3BG, England
Hardy, J.
Bhatia, K. P.
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Sobell Dept, Inst Neurol, London WC1N 3BG, England
UCL, Sobell Dept, Inst Neurol, London WC1N 3BG, England
Bhatia, K. P.
[
1
]
机构
:
[1]
UCL, Sobell Dept, Inst Neurol, London WC1N 3BG, England
[2]
Univ Lubeck, Dept Neurol, Schilling Dept Clin & Mol Neurogenet, Lubeck, Germany
来源
:
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
|
2009年
/ 80卷
/ 06期
基金
:
英国医学研究理事会;
关键词
:
HALLERVORDEN-SPATZ-SYNDROME;
THE-TIGER SIGN;
PHOSPHOLIPASE A(2);
DISEASE;
MUTATION;
PLA2G6;
DISORDERS;
D O I
:
10.1136/jnnp.2008.169953
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:589 / 590
页数:2
相关论文
共 21 条
[1]
The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome
Baumeister, FAM
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Baumeister, FAM
Auer, DP
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Auer, DP
Hörtnagel, K
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Hörtnagel, K
Freisinger, P
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Freisinger, P
Meitinger, T
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Meitinger, T
[J].
NEUROPEDIATRICS,
2005,
36
(03)
: 221
-
222
[2]
BOKRYSHA N, 2008, MULT SCLER, V14, P602
[3]
INHIBITION OF AUTOIMMUNE NEUROPATHOLOGICAL PROCESS BY TREATMENT WITH AN IRON-CHELATING AGENT
BOWERN, N
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
BOWERN, N
RAMSHAW, IA
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
RAMSHAW, IA
CLARK, IA
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
CLARK, IA
DOHERTY, PC
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
DOHERTY, PC
[J].
JOURNAL OF EXPERIMENTAL MEDICINE,
1984,
160
(05)
: 1532
-
1543
[4]
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease
Bras, Jose
论文数:
0
引用数:
0
h-index:
0
机构:
NIA, Mol Genet Unit, Bethesda, MD 20892 USA
Univ Coimbra, Ctr Neurosci & Cell Biol, P-3000 Coimbra, Portugal
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Bras, Jose
Singleton, Andrew
论文数:
0
引用数:
0
h-index:
0
机构:
NIA, Mol Genet Unit, Bethesda, MD 20892 USA
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Singleton, Andrew
Cookson, Mark R.
论文数:
0
引用数:
0
h-index:
0
机构:
NIA, Cell Biol & Gene Express Unit, Bethesda, MD 20892 USA
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Cookson, Mark R.
Hardy, John
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Inst Neurol, Dept Neurodegenerat Dis, London WC1N 3BG, England
Inst Neurol, Reta Lila Weston Inst, London WC1N 3BG, England
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Hardy, John
[J].
FEBS JOURNAL,
2008,
275
(23)
: 5767
-
5773
[5]
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
Curtis, ARJ
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Curtis, ARJ
Fey, C
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Fey, C
Morris, CM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Morris, CM
Bindoff, LA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Bindoff, LA
Ince, PG
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Ince, PG
Chinnery, PF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Chinnery, PF
Coulthard, A
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Coulthard, A
Jackson, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Jackson, MJ
Jackson, AP
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Jackson, AP
McHale, DP
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
McHale, DP
Hay, D
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Hay, D
Barker, WA
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0
引用数:
0
h-index:
0
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Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Barker, WA
Markham, AF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Markham, AF
Bates, D
论文数:
0
引用数:
0
h-index:
0
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Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Bates, D
Curtis, A
论文数:
0
引用数:
0
h-index:
0
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Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Curtis, A
Burn, J
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0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Burn, J
[J].
NATURE GENETICS,
2001,
28
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354
[6]
Gerlach M, 2006, J NEURAL TRANSM-SUPP, P133
[7]
Gregory A, 2005, FOLIA NEUROPATHOL, V43, P286, DOI 10.1016/B978-0-444-63233-3.00019-1
[8]
THE EFFECT OF AGE ON THE NON-HAEMIN IRON IN THE HUMAN BRAIN
HALLGREN, B
论文数:
0
引用数:
0
h-index:
0
HALLGREN, B
SOURANDER, P
论文数:
0
引用数:
0
h-index:
0
SOURANDER, P
[J].
JOURNAL OF NEUROCHEMISTRY,
1958,
3
(01)
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51
[9]
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
Hayflick, SJ
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Hayflick, SJ
Westaway, SK
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Westaway, SK
Levinson, B
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Levinson, B
Zhou, B
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Zhou, B
Johnson, MA
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Johnson, MA
Ching, KHL
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Ching, KHL
Gitschier, J
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Gitschier, J
[J].
NEW ENGLAND JOURNAL OF MEDICINE,
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[10]
PLA2G6 mutation underlies infantile neuroaxonal dystrophy
Khateeb, Shareef
论文数:
0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Khateeb, Shareef
Flusser, Hagit
论文数:
0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Flusser, Hagit
Ofir, Rivka
论文数:
0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Ofir, Rivka
Shelef, Ilan
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0
引用数:
0
h-index:
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Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Shelef, Ilan
Narkis, Ginat
论文数:
0
引用数:
0
h-index:
0
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Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Narkis, Ginat
Vardi, Gideon
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0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Vardi, Gideon
Shorer, Zamir
论文数:
0
引用数:
0
h-index:
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机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Shorer, Zamir
Levy, Rachel
论文数:
0
引用数:
0
h-index:
0
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Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Levy, Rachel
Galil, Aharon
论文数:
0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Galil, Aharon
Elbedour, Khalil
论文数:
0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Elbedour, Khalil
Birk, Ohad S.
论文数:
0
引用数:
0
h-index:
0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
Birk, Ohad S.
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2006,
79
(05)
: 942
-
948
←
1
2
3
→
共 21 条
[1]
The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome
Baumeister, FAM
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Baumeister, FAM
Auer, DP
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Auer, DP
Hörtnagel, K
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Hörtnagel, K
Freisinger, P
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Freisinger, P
Meitinger, T
论文数:
0
引用数:
0
h-index:
0
机构:
Tech Univ Munich, Childrens Hosp, D-80804 Munich, Germany
Meitinger, T
[J].
NEUROPEDIATRICS,
2005,
36
(03)
: 221
-
222
[2]
BOKRYSHA N, 2008, MULT SCLER, V14, P602
[3]
INHIBITION OF AUTOIMMUNE NEUROPATHOLOGICAL PROCESS BY TREATMENT WITH AN IRON-CHELATING AGENT
BOWERN, N
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
BOWERN, N
RAMSHAW, IA
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
RAMSHAW, IA
CLARK, IA
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
CLARK, IA
DOHERTY, PC
论文数:
0
引用数:
0
h-index:
0
机构:
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
AUSTRALIAN NATL UNIV,DEPT ZOOL,CANBERRA,ACT 2601,AUSTRALIA
DOHERTY, PC
[J].
JOURNAL OF EXPERIMENTAL MEDICINE,
1984,
160
(05)
: 1532
-
1543
[4]
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease
Bras, Jose
论文数:
0
引用数:
0
h-index:
0
机构:
NIA, Mol Genet Unit, Bethesda, MD 20892 USA
Univ Coimbra, Ctr Neurosci & Cell Biol, P-3000 Coimbra, Portugal
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Bras, Jose
Singleton, Andrew
论文数:
0
引用数:
0
h-index:
0
机构:
NIA, Mol Genet Unit, Bethesda, MD 20892 USA
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Singleton, Andrew
Cookson, Mark R.
论文数:
0
引用数:
0
h-index:
0
机构:
NIA, Cell Biol & Gene Express Unit, Bethesda, MD 20892 USA
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Cookson, Mark R.
Hardy, John
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Inst Neurol, Dept Neurodegenerat Dis, London WC1N 3BG, England
Inst Neurol, Reta Lila Weston Inst, London WC1N 3BG, England
UCL, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
Hardy, John
[J].
FEBS JOURNAL,
2008,
275
(23)
: 5767
-
5773
[5]
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
Curtis, ARJ
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Curtis, ARJ
Fey, C
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Fey, C
Morris, CM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Morris, CM
Bindoff, LA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Bindoff, LA
Ince, PG
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Ince, PG
Chinnery, PF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Chinnery, PF
Coulthard, A
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Coulthard, A
Jackson, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Jackson, MJ
Jackson, AP
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Jackson, AP
McHale, DP
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
McHale, DP
Hay, D
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Hay, D
Barker, WA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Barker, WA
Markham, AF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Markham, AF
Bates, D
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Bates, D
Curtis, A
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Curtis, A
Burn, J
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Human Genet, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
Burn, J
[J].
NATURE GENETICS,
2001,
28
(04)
: 350
-
354
[6]
Gerlach M, 2006, J NEURAL TRANSM-SUPP, P133
[7]
Gregory A, 2005, FOLIA NEUROPATHOL, V43, P286, DOI 10.1016/B978-0-444-63233-3.00019-1
[8]
THE EFFECT OF AGE ON THE NON-HAEMIN IRON IN THE HUMAN BRAIN
HALLGREN, B
论文数:
0
引用数:
0
h-index:
0
HALLGREN, B
SOURANDER, P
论文数:
0
引用数:
0
h-index:
0
SOURANDER, P
[J].
JOURNAL OF NEUROCHEMISTRY,
1958,
3
(01)
: 41
-
51
[9]
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
Hayflick, SJ
论文数:
0
引用数:
0
h-index:
0
机构:
Oregon Hlth Sci Univ, Dept Mol & Med Genet, Sch Med, Portland, OR 97201 USA
Hayflick, SJ
Westaway, SK
论文数:
0
引用数:
0
h-index:
0
机构:
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