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Author/Creator Beiraghi Toosi, Mehran

2. Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review. Issue 1 (23rd August 2022)

Authors:
Magrinelli, Francesca; Bhatia, Kailash P.; Beiraghi Toosi, Mehran; Arab, Fatemeh; Karimiani, Ehsan Ghayoor; Sedighzadeh, Sahar; Ansari, Behnaz; Neshatdoust, Maedeh; Rocca, Clarissa; Houlden, Henry; Maroofian, Reza
Journal:
Movement disorders clinical practice
Issue:
Volume 10:Issue 1(2023)
Page Start:
101
Record Type:
Journal Article
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3. Recurrent Painful Ophthalmoplegic Neuropathy with Unilateral Oculomotor and Trochlear Nerve Palsy in an 8-year-old Girl. Issue 4 (2nd October 2022)

Authors:
Akhondian, Javad; Ashrafzadeh, Farah; Seilanian Toosi, Farrokh; Esmaeilzadeh, Mahla; Beiraghi Toosi, Mehran; Imannezhad, Shima; Saeedi Zand, Nazanin; Hashemi, Narges
Journal:
Journal of binocular vision and ocular motility
Issue:
Volume 72:Issue 4(2022)
Page Start:
199
Record Type:
Journal Article
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4. The report of two cases with multiple sulfatase deficiency resulting from a rare similar gene mutation. (26th February 2018)

Authors:
Ashrafzadeh, Farah; Zabolinejad, Naghmeh; Ghayoor Karimiani, Ehsan; Beiraghi Toosi, Mehran; Doniadideh, Nahid; Torabi, Shatila; Razmyar, Mohammad; Sheikh Andalibi, Mohammad S.
Journal:
International journal of dermatology
Issue:
Volume 57:Number 10(2018)
Page Start:
1242
Record Type:
Journal Article
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5. TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition. Issue 9 (7th June 2022)

Authors:
Musante, Luciana; Faletra, Flavio; Meier, Kolja; Tomoum, Hoda; Najarzadeh Torbati, Paria; Blair, Edward; North, Sally; Gärtner, Jutta; Diegmann, Susann; Beiraghi Toosi, Mehran; Ashrafzadeh, Farah; Ghayoor Karimiani, Ehsan; Murphy, David; Murru, Flora Maria; Zanus, Caterina; Magnolato, Andrea; La ...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 9(2022)
Page Start:
2652
Record Type:
Journal Article
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