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Publisher : wolters kluwer india pvt ltd

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Academic Journal

Electrophysiological and radiological diagnosis of hereditary motor and sensory polyneuropathy.

Authors : Al‑Khlaiwi, Thamir¹ ; Meo, Imran²; Butt, Muhammad A.³

Source: Journal of Family Medicine & Primary Care. Jun2024, Vol. 13 Issue 6, p2511-2515. 5p.

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Academic Journal

Navigating the swells: A case report of hereditary angioedema.

Authors : Taori, Kamlesh¹ ; Kirnake, Vijendra¹; Junare, Parmeshwar¹

Source: Journal of Family Medicine & Primary Care. Jul2024, Vol. 13 Issue 7, p2784-2786. 3p.

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Academic Journal

Pontine Tegmental Cap Dysplasia: A Rare Brainstem Malformation Mimicking Hereditary Sensory Autonomic Neuropathy.

Authors : A. R., Nagaraj¹; Shravanthi, Guduru¹; Kumar, Tumulu Seetam²

Source: Annals of Indian Academy of Neurology. Mar/Apr2024, Vol. 27 Issue 2, p217-220. 4p.

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Academic Journal

Hereditary Sensory and Autonomic Neuropathy Type II in Two Brothers, a Close Differential of Leprosy.

Authors : Sachan, Sonal¹; Verma, Nishant²; Verma, Parul³

Source: Indian Journal of Paediatric Dermatology. Jan-Mar2023, Vol. 24 Issue 1, p68-71. 4p.

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Academic Journal

Changes in visual acuity using low vision devices in patients with Leber hereditary optic neuropathy: A retrospective study.

Authors : Gopalakrishnan, Sarika¹ (AUTHOR); Bhaskaran, Gnanapoonkodi² (AUTHOR); Jayasankar, Ompriya³ (AUTHOR)

Source: Indian Journal of Ophthalmology. Feb2023, Vol. 71 Issue 2, p402-407. 6p.

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Academic Journal

May--Hegglin anomaly: A rare hereditary autoimmune thrombocytopenia.

Authors : Singh, Vinaya¹ ; Khan, Mazhar Nasir¹; Malik, Sushma¹

Source: Indian Journal of Health Sciences & Biomedical Research KLEU. May-Aug2023, Vol. 16 Issue 2, p316-319. 4p.

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Academic Journal

Clinical Profile of Patients with Leber Hereditary Optic Neuropathy (LHON): An Ambispective Study of North Indian Cohorts.

Authors : Wilson, Vinny¹; Kaur, Prabhjit²; Singh, Sofia²

Source: Annals of Indian Academy of Neurology. 2022 Supplement, Vol. 25, p65-69. 5p.

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Academic Journal

Hereditary Antithrombin Deficiency Presenting with Cerebral Venous Thrombosis in Three Members of a Family.

Authors : Ashraf, V. V.¹ ; Salam, K. Abdul¹; Kizhedath, Rajesh²

Source: Neurology India. Sep/Oct2023, Vol. 71 Issue 5, p984-986. 3p.

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Academic Journal

Severe pulmonary arterial hypertension in a patient with hereditary hemorrhagic telangiectasia and multiple pulmonary and hepatic arteriovenous malformations.

Authors : Aramalla, Sunitha¹; Bhyravavajhala, Srinivas¹; Vanaparty, Bharathi¹

Source: Annals of Pediatric Cardiology. Jan/Feb2022, Vol. 15 Issue 1, p73-76. 4p.

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Academic Journal

Painless self-mutilation − A case of hereditary sensory autonomic neuropathy type 4.

Authors : Pathak, Prateek¹ (AUTHOR); Adil, Mohammad¹ (AUTHOR); Amin, Syed¹ (AUTHOR)

Source: Indian Journal of Paediatric Dermatology. Jan-Mar2022, Vol. 23 Issue 1, p67-70. 4p.

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نتائج البحث

فلترة النتائج

Electrophysiological and radiological diagnosis of hereditary motor and sensory polyneuropathy.

Navigating the swells: A case report of hereditary angioedema.

Pontine Tegmental Cap Dysplasia: A Rare Brainstem Malformation Mimicking Hereditary Sensory Autonomic Neuropathy.

Hereditary Sensory and Autonomic Neuropathy Type II in Two Brothers, a Close Differential of Leprosy.

Changes in visual acuity using low vision devices in patients with Leber hereditary optic neuropathy: A retrospective study.

May--Hegglin anomaly: A rare hereditary autoimmune thrombocytopenia.

Clinical Profile of Patients with Leber Hereditary Optic Neuropathy (LHON): An Ambispective Study of North Indian Cohorts.

Hereditary Antithrombin Deficiency Presenting with Cerebral Venous Thrombosis in Three Members of a Family.

Severe pulmonary arterial hypertension in a patient with hereditary hemorrhagic telangiectasia and multiple pulmonary and hepatic arteriovenous malformations.

Painless self-mutilation − A case of hereditary sensory autonomic neuropathy type 4.

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